Cody H. v. State of New York

2025 NY Slip Op 25162
CourtNew York Court of Claims
DecidedJune 16, 2025
DocketClaim No. 137291
StatusPublished

This text of 2025 NY Slip Op 25162 (Cody H. v. State of New York) is published on Counsel Stack Legal Research, covering New York Court of Claims primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Cody H. v. State of New York, 2025 NY Slip Op 25162 (N.Y. Super. Ct. 2025).

Opinion

Cody H. v State of New York (2025 NY Slip Op 25162) [*1]

Cody H. v State of New York
2025 NY Slip Op 25162
Decided on June 16, 2025
Court Of Claims
Calderon, J.
Published by New York State Law Reporting Bureau pursuant to Judiciary Law § 431.
This opinion is uncorrected and subject to revision before publication in the printed Official Reports.


Decided on June 16, 2025
Court of Claims


Cody H. and BRITTANY H., Individually and as parents and natural guardians of A.H., an Infant, Claimants,

against

The State of New York, Defendant.




Claim No. 137291

For Claimants:
STEVE FOLEY LAW
By: Stephen R. Foley, Esq.

For Defendant:
LETITIA JAMES, Attorney General of the State of New York
By: Michael T. Feeley, Assistant Attorney General
Francisco Calderon, J.

The tragic facts of this case are largely undisputed. In March 2021, claimant Brittany H. gave birth to her and claimant Cody H.'s first child, claimant A.H. Shortly thereafter, a blood sample was taken from A.H. for the State's Newborn Screening Program—an initiative started by the state in the 1960s that now tests for over 50 conditions, including spinal muscular atrophy (SMA). A.H.'s sample screened positive for SMA. However, due to a transcriptional error, A.H.'s pediatrician was sent a report indicating that A.H. did not screen positive for any of the tested conditions. A few months after her birth, A.H. began experiencing the symptoms of SMA and was subsequently diagnosed with such. However, because A.H. did not begin treatment until after her symptoms manifested, the deleterious effects of her condition could not be averted.

Claimants commenced this action, alleging that defendant is negligent for inaccurately relaying the results of A.H.'s screening. Defendant answered, raising 23 affirmative defenses. Claimants now move, following discovery, to strike all of defendant's affirmative defenses. [*2]Defendant opposes the motion and cross-moves for summary judgment to dismiss the claim. Claimants oppose defendant's cross-motion. The parties were permitted to supplement their papers in response to the Court of Appeals' decision in Weisbrod-Moore v Cayuga County (___ NY3d ___, 2025 NY Slip Op 00903 [2025]). The Court heard the parties for oral argument on April 23, 2025. For the reason's stated below, claimants' motion to strike defendant's affirmative defenses is denied and defendant's cross-motion for summary judgment is granted.

FACTUAL BACKGROUND

In support of their motion, claimants submit, among other exhibits, the depositions of Michele Caggana, Brittany H., and Cody H.; the original and corrected reports with A.H.'s screening results; reports generated by the Wadsworth Center in relation to this incident; the brochure about the newborn screening program given to parents; and excerpts from the Wadsworth Center's website.

As stated in her deposition, Dr. Michele Caggana is the Deputy Director for the Division of Genetics, Director of the Newborn Screening Program, and Chief of the Laboratory of Human Genetics at the Wadsworth Center, a division of the Department of Health. Dr. Caggana relayed that the newborn screening program began in 1965 to test for a condition known as phenylketonuria. Since then, the program has expanded to test for numerous disorders that, if discovered early, can be effectively treated. This testing is compulsory pursuant to the Public Health Law absent a religious exception. All parents with newborns receive a brochure explaining what the genetic testing involves and that their doctor will receive a report with the results. The testing is conducted at the Wadsworth Center. Dr. Caggana explained, and as supplemented by the Wadsworth Center's website, that one of the conditions covered by the program is SMA, which is a genetic neuromuscular disorder that can be effectively treated before symptoms develop. If the condition is not uncovered early, a child with SMA will manifest symptoms within a few months and suffer permanent muscle degeneration.

Dr. Caggana first learned of A.H. when she was contacted by a physician treating her who suspected that she had SMA. Dr. Caggana conducted an investigation and discovered that, although A.H. had tested positive for SMA, the control value for the test had been accidentally entered into the results column. Therefore, although A.H. should have screened positive for SMA, she instead received a negative report. After this was uncovered, a new report for A.H. was generated indicating that she was positive for SMA.

While Dr. Caggana stated that the tests are reliable, she also stressed that the screening program is not intended to be a diagnostic test. In other words, even if an infant screens positive for a condition, they should not be diagnosed until follow-up testing is performed by the infant's pediatrician. Both the brochure given to parents and the Wadsworth Center website warn that a negative screen does not necessarily mean an infant will be healthy, with the latter stating that "[p]arents should not be told that a negative screen rules out SMA" (Wadsworth Ctr Website Excerpts, Affirm in Supp of Mot, Exh K, 17 [emphasis in original]). Similarly, the screening report received by pediatricians states that "[t]hese tests are not diagnostic" (Negative Report, id., Exh D, 2).

During her deposition testimony, Ms. H. stated that she brought A.H. to see her pediatrician within one week of her birth. At that time, the pediatrician indicated that A.H. was healthy. However, approximately two months after her birth, the pediatrician began to have concerns about A.H.'s muscular development and recommended that she see a neurologist. Eventually, A.H. was diagnosed with SMA. Ms. H. was told by the physician that, had A.H. [*3]been diagnosed earlier, she likely would not have developed symptoms of SMA. A.H. began treatment shortly after her diagnosis. However, she requires use of a wheelchair, cannot crawl or walk, and cannot transition from one body position to another on her own. She also requires extensive physical therapy every week. Mr. H.'s deposition confirmed Ms. H.'s recounting of events.

Claimants also submitted the affirmation of Abigail Schwaede, M.D., a doctor with board certification in neurology and special qualification in child neurology. Dr. Schwaede averred that, if SMA is diagnosed early, infants can be treated before the onset of symptoms and without negative effects. However, because A.H. was diagnosed after the onset of symptoms, she suffered from permanent neuromuscular deficits that could have been avoided had she started treatment earlier.

In response, defendant submitted an affirmation from Dr. Caggana and the test result from a private laboratory in which A.H. was diagnosed with SMA. In her affirmation, Dr. Caggana provided more information about the screening program. In particular, she stated that New York is one of only two states that does not charge for newborn screening services and that the program is instead funded through a suballocation by the Department of Financial Services, with a 2023-2024 allotment of $14,088,017. Between 205,000 and 227,000 infants are tested each year through the program, resulting in the State reporting around 1.7 million test results over the course of six years. The program began testing for SMA in 2018 following a two-year pilot study.



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2025 NY Slip Op 25162, Counsel Stack Legal Research, https://law.counselstack.com/opinion/cody-h-v-state-of-new-york-nyclaimsct-2025.