Opinion

Correira v. Secretary of Health and Human Services

Court
United States Court of Federal Claims
Filed
Jul 8, 2025
Status
Unpublished
On the bench
Brian H. Corcoran
Cited by
0 cases
Authority
More cited than 37.4%

“We generally presume that a special master considered the relevant record evidence even though he does not explicitly reference such evidence in his decision.”

How later courts described this case

  • “We generally presume that a special master considered the relevant record evidence even though he does not explicitly reference such evidence in his decision.”
  • explaining that a special master must decide what weight to give evidence including oral testimony and contemporaneous medical records
  • affirming the special master's reliance on findings of the IOM
  • noting that “it was appropriate for the special master to consider the medical literature presented, including the IOM report” and that “the court often has relied on the findings of the Institute of Medicine.”

Written by the judges who cited it.

The opinion

In the United States Court of Federal Claims

OFFICE OF SPECIAL MASTERS

No. 22-1269V

UNPUBLISHED

ALAN CORREIRA, Chief Special Master Corcoran

Petitioner, Filed: June 3, 2025

v.

SECRETARY OF HEALTH AND

HUMAN SERVICES,

Respondent.

Ronald Craig Homer, Conway, Homer, P.C., Boston, MA, for Petitioner.

James Vincent Lopez, U.S. Department of Justice, Washington, DC, for Respondent.

DECISION 1

On August 27, 2021, Alan Correira filed a petition for compensation under the

National Vaccine Injury Compensation Program, 42 U.S.C. §300aa-10, et seq. 2 (the

“Vaccine Act”). Petitioner alleges that he received an influenza (“flu”) vaccine on

September 20, 2019, and thereafter suffered Guillain-Barré syndrome (“GBS”) that was

caused in fact by the vaccination. Amended Petition at 1. The case was assigned to the

Special Processing Unit of the Office of Special Masters. For the reasons discussed

below, this claim is hereby DISMISSED.

1 Because this unpublished fact ruling contains a reasoned explanation for the action in this case, I am

required to post it on the United States Court of Federal Claims' website in accordance with the E-

Government Act of 2002. 44 U.S.C. § 3501 note (2012) (Federal Management and Promotion of Electronic

Government Services). This means the fact ruling will be available to anyone with access to the

internet. In accordance with Vaccine Rule 18(b), petitioner has 14 days to identify and move to redact

medical or other information, the disclosure of which would constitute an unwarranted invasion of privacy.

If, upon review, I agree that the identified material fits within this definition, I will redact such material from

public access.

2 National Childhood Vaccine Injury Act of 1986, Pub. L. No. 99-660, 100 Stat. 3755. Hereinafter, for ease

of citation, all section references to the Vaccine Act will be to the pertinent subparagraph of 42 U.S.C. §

300aa (2012).

I. Procedural History

After the claim’s initiation, Petitioner filed an amended petition with citations to the

record. Amended Petition (“petition”), ECF No. 18. Respondent filed a Rule 4(c) Report

opposing compensation, arguing Petitioner has not provided a medical or scientific

showing that the vaccination caused his alleged GBS. Respondent’s Rule 4(c) Report

(“Res. Rep”) ECF No. 21, at 1. Petitioner was ordered to show cause why this case should

not be dismissed. ECF No. 24. The order noted that onset of Petitioner’s GBS appeared

to have occurred outside the longest time accepted for a non-table flu/GBS claim. Id.

Petitioner filed his response and additional evidence on September 12, 2023.

Petitioner’s Response to the Court’s August 1, 2023 Show Cause Order (“Pet. Res.”),

ECF No. 27. Petitioner argues that he has established a prima facie case for causation.

Id. at 22-31.

II. Fact History

a. Medical Records

Petitioner received a flu vaccine on September 20, 2019. Ex. 1 at 1. Ten days later,

he underwent prostate surgery that involved nitrous oxide. Ex. 8 at 6 (noting that Petitioner

had prostate surgery on October 1, 2019).

On November 23, 2019, Petitioner sought care at the emergency department. Ex.

7 at 5-8. He complained of numbness and tingling in his bilateral upper extremities that

began on November 18, 2019, and “[c]onstant sensation for the past 6 days.” Id. A

physical exam was unremarkable, and he was diagnosed with bilateral upper extremity

neuropathy. Id.

On November 26, 2019, Petitioner saw his primary care physician, Dr. Irvin, for a

follow-up. Ex. 2 at 26-27. He reported numbness in his upper extremities, feet, tongue,

and lips, but denied weakness. Id. Petitioner also stated that his symptoms had improved

over the past three days, but were still present. Id. An examination showed normal gait,

and no motor or sensory deficits. Petitioner was assessed with paresthesia of unclear

etiology. Id.

Petitioner saw Dr. Leber, a neurologist, on November 27, 2019, for numbness in

his forearms, tongue, and left foot. Ex. 8 at 6. He stated that on November 18, 2019, he

woke with his hands and forearms feeling cold and somewhat numb. Id. He also reported

the prostate surgery on October 1, 2019, which Dr. Leber noted could cause myelopathy

in patients with previous anemia. Id. A neurologic exam was “basically unremarkable,”

but he recorded a slight Bell’s palsy of the left eyelid and mild absent sensation in the

right foot. Id. at 7. Dr. Leber noted that due to the sudden onset of numbness, “one has

to think of cervical myelopathy or cervical issues.” Id. at 7-8. A subsequent MRI was

unremarkable. Id. 15-16. Additionally, his B12 and folic acid were within normal limits. Id.

at 10.

Petitioner returned to Dr. Leber on December 6, 2019, reporting recent onset of

stumbling, slurring speech and tingling in his face and scalp. Ex. 8 at 10. Dr. Leber noted

there was “no objective abnormality on examination, other than residual from previous

left Bell’s palsy.” Id. He also stated he could not explain the described subjective sensory

symptoms, and prescribed alprazolam for his anxiety. Id.

Later on December 6, 2019, Petitioner was seen at the emergency department for

increased left facial droop that started that morning. Ex. 3 at 32. He was diagnosed with

Bell’s palsy. Id. at 35-36. Three days later, on December 9, 2019, Petitioner saw his

primary care physician. Ex. 9 at 9. A physical and neurologic examination was

unremarkable, but he was referred to a neurologist for a second opinion. Id. at 10.

Petitioner returned to the emergency department on December 12, 2019,

complaining of numbness throughout his body, upper extremity pain, dizziness, and

difficulty walking that started just prior to his arrival. Ex. 4 at 575. He showed left sided

facial droop, absent bilateral reflexes, and an abnormal gait. Id. at 578. A lumbar puncture

showed elevated protein levels. Id. at 752. The admitting physician noted that Petitioner

“had a flu shot back in September. Question progressive [GBS] versus Lambert-Eaton

syndrome.” Id. at 403.

An addendum from December 13, 2019, states that Petitioner reported only

subjective symptoms, and no objective abnormalities could be observed. But Dr.

Khademi, a neurologist, could not rule out the possibility of an autoimmune neuropathy,

“[i]n this case [GBS], predominantly sensory variant….” Ex. 4 at 1451. Dr. Khademi also

noted that the nadir of the weakness is usually 3-4 weeks from onset. Id. at 1451, 416.

Petitioner was discharged on December 14, 2019, with possible diagnoses including GBS

and Labert-Eaton syndrome, an autoimmune neurological condition. Ex. 7 at 9-10.

A follow-up on December 16, 2019, with Dr. Irvin included a suspected diagnoses

of the “predominantly sensory form” of GBS. Ex. 2 at 30-31. Petitioner saw Dr. Khademi

for a second opinion on December 20, 2019. Ex. 5 at 9-10. An examination showed

absent reflexes, left peripheral facial weakness, impaired gait, reduced sensation, but

normal motor strength. Id. He was assessed with inflammatory polyneuropathy and

possible GBS. Id.

On December 21, 2019, Petitoiner returned to the emergency department for

worsening paresthesia, and trouble breathing and swallowing. Ex. 4 at 1052. He exhibited

decreased sensation in his trunk and chest, decreased grip strength, left sided facial

droop, and absent reflexes. Id. at 1055. The differential diagnosis included GBS versus

variant, a more chronic condition such as chronic demyelinating syndrome, and Eaton-

Lambert syndrome. Id.

Petitioner saw another neurologist, Dr. Huntley, on December 21, 2019, reporting

a five-week history of progressive weakness. Ex. 4 at 836. An examination showed

“wildly” uncontrolled ambulation and absent reflexes. Id. at 837. He was assessed with

paresthesia, dysphagia, a history of Bell’s palsy with gait disorder. Id. at 837. Dr. Huntley

also noted that he had “a hard time piecing this all together. The patient tells me Dr.

Khademi was ordering IVIG, but it had not been set up yet…. I am wondering if he really

needs IVIG.” Id. at 837-38. Results from an EMG/NCS on December 24, 2019 were

consistent with neuropathy with demyelinating and axonal components “in the family of

GBS.” Id. at 386. Dr. Huntley noted this was a “[f]ascinating case, a lot of overly but at

the core [Petitioner] has [GBS].” Id. at 850.

Petitioner underwent a five-day course of IVIG, and was discharged on December

26, 2019. Ex. 4 at 79. Thereafter, Petitioner’s symptoms improved. Ex. 2 at 37 (follow-up

on December 30, 2019 stating symptoms have improved since his discharge); Ex. 9 at

12 (record from March 20, 2020, stating that Petitioner has improved approximately 80%).

By May 20, 2020, he reported some residual numbness but also significant improvement

to Dr. Vasquez, a neurologist. Ex. 6 at 8. Dr. Vasquez noted he had no flu-like symptoms

before onset, no diarrhea, but he “did have a flu shot in September of last year.” Ex. 6 at

8.

b. Affidavit Evidence

Petitioner submitted an affidavit in support of his claim on March 6, 2023. Ex. 12.

Petitioner states that he received a flu vaccine on September 20, 2019. Id. at 1. He began

experiencing numbness in his hands in November of 2019, although he could not recall

the precise onset date. Id. Additionally, he states that he “did experience worsening

symptoms for at least one week before seeking care….” Id.

c. Expert Report

Petitioner submitted an expert report from Dr. Norman Latov, M.D., Ph.D (“Ex.

Rep.), dated July 24, 2023. Dr. Latov attended the University of Pennsylvania to complete

his medical and doctorate degree. Ex. 15 at 1. He completed his residency in neurology

and immunology at Columbia University and is now on the faculty at Weill Cornell

Medicine. Id. at 3. Dr. Latov directs a peripheral neuropathy center as well as serving as

a professor of neurology and neuroscience, and being an attending neurologist. Id., Ex.

Rep. at 2. In his clinical practice he has “devoted a substantial portion … to the evaluation,

diagnosis, and treatment of patients with peripheral neuropathies including Guillain–Barré

syndrome (GBS) chronic inflammatory demyelinating polyneuropathy (CIDP). Id.

Dr. Latov opined that that vaccines can induce autoimmune disease such as GBS

through molecular mimicry or bystander activation. Ex. Rep. at 5-6. Both molecular

mimicry and bystander activation have been accepted by the Institute of Medicine

(“IOM”)10 as possible explanations for post-vaccination adverse events. Id. (citing

INSTITUTE OF MEDICINE, ADVERSE EFFECTS OF VACCINES: EVIDENCE AND

CAUSALITY 57 (Stratton et al. eds., 2012) [hereinafter 2012 IOM Report] (Ex. 25)). 3 By

Dr. Latov's description “[m]olecular mimicry occurs when there is a structural homology,

in sequence or conformation, between an exogenous agent, such as a vaccine or

infection, and a self or autoantigen that is subsequently targeted by the immune response.

Induction of immune reactivity against the foreign agent results in cross reactivity with the

self-antigen, with subsequent tissue damage and autoimmune disease.” Id. at 6.

Regarding bystander activation, he observes that the normal immune state incudes auto-

reactive cells that are suppressed by immune tolerance, thereby preventing autoimmune

3

The Institute of Medicine (known as the National Academy of Medicine since 2015) is the medical arm of

the National Academy of Sciences. The National Academy of Sciences (“NAS”) was created by Congress

in 1863 to be an advisor to the federal government on scientific and technical matters (see An Act to

Incorporate the National Academy of Sciences, ch. 111, 12 Stat. 806 (1863)), and the Institute of Medicine

is an offshoot of the NAS established in 1970 to provide advice concerning medical issues. When it enacted

the Vaccine Act in 1986, Congress directed that the IOM conduct studies concerning potential causal

relationships between vaccines and illnesses. See § 300aa–1. However, the IOM employs a standard for

finding causation that is higher than what is required by petitioner's burden of proof. E.g. Raymo v. Sec'y

of Health & Hum. Servs., No. 11-654V, 2014 WL 1092274, at *21, n. 39 (Fed. Cl. Spec. Mstr. Feb. 24,

2014). Accordingly, IOM reports and findings should be approached with caution. Special Masters may rely

on IOM reports as evidence, but they are not dispositive. See, e.g., Crutchfield v. Sec'y Health & Hum.

Servs., 125 Fed. Cl. 251, 262 (2014) (noting that “it was appropriate for the special master to consider the

medical literature presented, including the IOM report” and that “the court often has relied on the findings

of the Institute of Medicine.”); see also, Isaac v. Sec'y Health & Hum. Servs., 108 Fed. Cl. 743, 755 (2013),

aff'd, 540 Fed. Appx. 999 (Mem.) (Fed. Cir. 2013) (affirming the special master's reliance on findings of the

IOM); Porter v. Sec'y Health & Hum. Servs., 663 F.3d 1242, 1252 (Fed.Cir.2011) (noting the special

master's comment that “IOM reports are favored, although not dispositive, in the Vaccine Act Program,”

then affirming the special master's decision).

disease. Bystander activation occurs when infection or immunization stimulate the

immune system in such a way as to overcome that immune tolerance. Id.

In petitioner's case, Dr. Latov observed, GBS most likely developed on or around

November 16, 2019, or 57-59 days post vaccination. Ex. Rep. at 7. According to Dr. Latov,

this is within the time period of elevated risk for developing GBS due to a vaccine. Id. To

support this conclusion, Dr. Latov cited a study that examined incidences of GBS

following a 1976 program for vaccination against the swine flu. Id. That study found that

most post-vaccination GBS cases occurred within five weeks of vaccination, but also

observed an increased risk lasting up to nine or ten weeks. L. Schonberger et al., Guillain-

Barré Syndrome Following Vaccination in the National Influenza Program, United States,

1976-77, 110 Am. J. Epid. 2:105-123 (1979), filed as Ex. 13.

Additionally, Dr. Latov concluded it is logical that Petitioner developed GBS as a

consequence of his vaccination. Ex. Rep. at 8. And he noted that there were no other

potential causes identified that could have triggered his GBS. Id.

III. Legal Standard

Before compensation can be awarded under the Vaccine Act, a petitioner must

demonstrate, by a preponderance of evidence, all matters required under Section

11(c)(1), including the factual circumstances surrounding his claim. Section 13(a)(1)(A).

In making this determination, the special master or court should consider the record as a

whole. Section 13(a)(1). Petitioner’s allegations must be supported by medical records or

by medical opinion. Id.

To resolve factual issues, the special master must weigh the evidence presented,

which may include contemporaneous medical records and testimony. See Burns v. Sec'y

of Health & Hum. Servs., 3 F.3d 415, 417 (Fed. Cir. 1993) (explaining that a special

master must decide what weight to give evidence including oral testimony and

contemporaneous medical records). Accordingly, where medical records are clear,

consistent, and complete, they should be afforded substantial weight. Lowrie v. Sec’y of

Health & Hum. Servs., No. 03-1585V, 2005 WL 6117475, at *20 (Fed. Cl. Spec. Mstr.

Dec. 12, 2005). However, the Federal Circuit has recently “reject[ed] as incorrect the

presumption that medical records are always accurate and complete as to all of the

patient’s physical conditions.” Kirby v. Sec'y of Health & Hum. Servs., 997 F.3d 1378,

1383 (Fed. Cir. 2021). Medical professionals may not “accurately record everything” that

they observe or may “record only a fraction of all that occurs.” Id.

In addition to requirements concerning the vaccination received, the duration and

severity of petitioner’s injury, and the lack of other award or settlement, 4 a petitioner

must establish that he suffered an injury meeting the Table criteria (i.e. a Table injury),

in which case causation is presumed, or an injury shown to be caused-in-fact by the

vaccination she received. If a petitioner cannot establish a Table injury, he or she may

pursue causation-in-fact under the legal standard set forth in Althen v. Sec'y of Health

& Human Servs., 418 F. 3d 1274, 1278 (Fed. Cir. 2005): “(1) a medical theory causally

connecting the vaccination and the injury; (2) a logical sequence of cause and effect

showing that the vaccination was the reason for the injury; and (3) a showing of

proximate temporal relationship between vaccination and injury.”

The association between the flu vaccine and GBS is well-established in the

Vaccine Program. See, e.g., Strong v. Sec'y of Health & Human Servs., No. 15-1108V,

2018 WL 1125666 (Fed. Cl. Spec. Mstr. Jan. 12, 2018); Stitt v. Sec'y of Health & Human

Servs., No. 09-653V, 2013 WL 3356791 (Fed. Cl. Spec. Mstr. May 31, 2013); Stewart

v. Sec'y of Health & Human Servs., No. 06-777V, 2011 WL 3241585, at *16 (Fed. Cl.

Spec. Mstr. July 8, 2011); see also Barone v. Sec'y of Health & Human Servs., No. 11-

707V, 2014 WL 6834557 (Fed. Cl. Spec. Mstr. Nov. 12, 2014). Indeed, GBS was added

in 2017 as a Table Claim for the flu vaccine (although this case does not involve such

a claim). See 42 C.F.R. § 100.3(a). Accordingly, my resolution of Petitioner's claim does

not turn on a finding, under Althen prong one, that (for purposes of adjudicating a

Program claim) the flu vaccine “can cause” GBS, for that question has been thoroughly

examined and answered in the affirmative.

There are nevertheless limits to the kinds of fact patterns that successfully

establish that the flu vaccine “did cause” a particular petitioner's GBS under the second

Althen prong. In most successful non-Table cases, onset of symptoms is demonstrated

to have occurred no longer than six to eight weeks after vaccination. See, e.g., Barone,

2014 WL 6834557, at *13 (eight weeks is the longest reasonable timeframe for a

flu/GBS injury). This means up to 56 days.

4

In summary, a petitioner must establish that he received a vaccine covered by the Program, administered

either in the United States and its territories; suffered the residual effects of his injury for more than six

months, died from his injury, or underwent a surgical intervention during an inpatient hospitalization; and

has not filed a civil suit or collected an award or settlement for his injury. See § 11(c)(1)(A)(B)(D)(E).

IV. Petitioner's GBS Onset Occurred Too Long After His Receipt of the Flu

Vaccine to Satisfy the Third Althen Prong5

Petitioner asserts that he is entitled to compensation because he has established

a prima facie case that his injury was caused-in-fact by the flu vaccine and has satisfied

the Althen prongs. Pet. Res. at 23-31. The following factual findings are made after a

complete and thorough review of the record, including all medical records, affidavits,

and all other additional evidence and filings from the parties. 6

The third Althen prong requires establishing a “proximate temporal relationship”

between the vaccination and the injury alleged. Althen, 418 F.3d at 1281. A petitioner

must offer “preponderant proof that the onset of symptoms occurred within a timeframe

for which, given the medical understanding of the disorder's etiology, it is medically

acceptable to infer causation.” Bazan v. Sec'y of Health & Human Servs., 539 F.3d 1347,

1352 (Fed. Cir. 2008).

In this case, Petitioner’s expert frames his discussion of onset in reference to a

study examining an outbreak of GBS following administration of the 1976 swine flu

vaccine – Schonberger, et al., (Ex. 14 at 6 (citing Schonberger). The medical literature

offered in this case establishes that a reasonable timeframe for onset of GBS after

vaccine administration would be no more than six to eight weeks, however. Schonberger

at 105. Specifically, Schonberger indicates that most GBS cases after the flu vaccine that

it evaluated occurred around 13-17 days, with their latest happening 41 days. Id. at 112.

This is echoed by the timeframe set for the Table version of the claim (see 42 C.F.R. §

100.3 (2017)). (It is in fact arguably the case that any onsets that exceed the 3-42 day

timeframe are suspect from a medical/scientific standpoint, since the onset timeframe is

specifically engineered to be over-inclusive, rather than to reflect a precise framework in

which a vaccine can, or cannot, cause injury).

5 As already noted, I do not include an extended discussion of the first Althen prong (which Petitioner

effectively satisfied). I also do not engage in an extended Althen prong two analysis, given my determination

that the timeframe for onset of Petitioner's GBS was too remote from vaccination to be deemed medically

reasonable. See, e.g., Hunt v. Sec'y of Health & Human Servs., 123 Fed. Cl. 509, 524-25 (2015) (citing

Veryzer v. Sec'y of Health & Human Servs., 100 Fed. Cl. 344, 355-56, aff'd, 475 F. App'x 765 (Fed. Cir.

2012) ). However, I note that the record does not conclude that the flu vaccine “did cause” Petitioner's GBS.

His symptoms do not reflect the manner in which GBS most commonly would progress. He initially reported

no motor or sensory deficits, showed some improvements shortly after reporting numbness, and exhibited

little objective abnormalities prior to December 6, 2019.

6

Though every document is not specifically referenced in this ruling, the complete record was reviewed and

considered. See Moriarty ex rel. Moriarty v. Sec’y of Health & Human Servs., 844 F.3d 1322, 1328 (Fed.

Cir. 2016) (“We generally presume that a special master considered the relevant record evidence even

though he does not explicitly reference such evidence in his decision.”).

Here, contemporaneous medical records preponderantly establish that the initial

symptoms of Petitioner’s GBS did not occur before November 18, 2019, 59 days after

his vaccination. Thus, when he presented to the hospital on November 23, 2019,

Petitioner complained of numbness and tingling in his extremities that began on

November 18, 2019, and had “[c]onstant sensation” for the past six days. Ex. 7 at 5-8.

He repeated this timeline on November 27, 2019. Ex. 8 at 6. This evidence outweighs

the record interpretation proposed by Dr. Latov for a slightly earlier onset (and I am not

obligated to accept his ipse dixit on this point). Ex. 14 at 6 (arguing that Petitioner’s

symptoms began 57-59 days after vaccination).

Measuring from the September 20, 2019 vaccination, then, a Table version of the

claim in this case could only succeed if onset had occurred on or before November 1,

2019 – which clearly did not occur. But even a causation-in-fact claim would have needed

to be based on symptoms beginning no more than two weeks after – or by November 15,

2019, at the latest. This also did not occur.

These facts accordingly are inconsistent with even the longest timeframes (eight

weeks) accepted for a similar non-Table claims recognized in reasoned Program

decisions. 7 See, e.g., Barone, 2014 WL 6834557, at *13. Petitioner’s onset thus occurred

far too long after vaccination to be considered “medically acceptable to infer causation-

in-fact.” See de Bazan, 539 F.3d at 1352; De La Cruz v. Sec'y of Health & Hum. Servs.,

No. 17-783V, 2018 WL 945834, at *1 (Fed. Cl. Jan. 23, 2018) (finding onset of GBS more

than two months after flu vaccination to be not compensable under either a theory of

causation in fact or significant aggravation).

7

Admittedly, other special masters have accepted a comparably-lengthy timeframe. See, e.g., Cooper v. Sec'y of

Health & Hum. Servs., No. 18-1885V, 2024 WL 1522331, at *20 (Fed. Cl. Mar. 12, 2024) (finding 60-day onset of GBS

following a vaccination allows inference of causation); Spayde v. Sec'y of Health & Hum. Servs., No. 16-1499V, 2021

WL 686682, at *19 (Fed. Cl. Jan. 27, 2021). But such decisions do not control this outcome. Moreover, they either

involve a different vaccine (for Cooper, the pneumococcal vaccine), or were based on reasoning that justified

stretching the eight-week timeframe a few days, in the interests of the Program’s emphasis on generosity and a

desire not to apply a hard, bright-line “rule.” Spayde, 2021 WL 686682, at *19. Of course, the proposed up-to-eight

weeks timeframe itself already exceeds the “rule” of the Table claim for the flu vaccine, and does not itself constitute

something that can be deemed accepted as a general matter. Moreover, this thinking reflects a logic whereby any

onset not shown to be facially impossible (say, more than 90 days) should be deemed medically acceptable. I do not

consider that kind of reasoning consistent with the science applicable to how vaccines are thought to cause GBS,

and it is not demanding scientific certainty to reject it.

Conclusion

The evidentiary record does not support Petitioner's contention that his GBS began

in a medically-acceptable timeframe after vaccination. Petitioner has thus not established

entitlement to a damages award, and therefore I must DISMISS his claim.

In the absence of a timely-filed motion for review (see Appendix B to the

Rules of the Court), the Clerk shall enter judgment in accordance with this

Decision. 8

IT IS SO ORDERED.

s/Brian H. Corcoran

Brian H. Corcoran

Chief Special Master

8

If Petitioner wishes to bring a civil action, he must file a notice of election rejecting the judgment pursuant

to § 21(a) “not later than 90 days after the date of the court’s final judgment.”

This is a copy of a public record, reproduced as it was published. It is not legal advice, and it may not be the version a court would rely on. Check the official source before you cite it.

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