Stradis Healthcare, LLC v. Geri-Care Pharmaceuticals Corporation

Court of Appeals for the Fourth Circuit·Decided July 16, 2025·No. 23-1246·Published

Opinion

PUBLISHED

UNITED STATES COURT OF APPEALS FOR THE FOURTH CIRCUIT

No. 23-1181

KERALINK INTERNATIONAL, INC., Plaintiff,

v. STRADIS HEALTHCARE, LLC, Defendant and Third-Party Plaintiff – Appellee, v. GERI-CARE PHARMACEUTICALS CORPORATION, Third-Party Defendant – Appellant, and INSOURCE, INC.; KAREWAY PRODUCT, INC., Third-Party Defendants.

No. 23-1246

KERALINK INTERNATIONAL, INC., Plaintiff,

v. STRADIS HEALTHCARE, LLC,

Defendant and 3rd-Party Plaintiff – Appellant, v. GERI-CARE PHARMACEUTICALS CORPORATION,

Third Party Defendant – Appellee, and

INSOURCE, INC.; KAREWAY PRODUCT, INC., Defendants.

Appeal from the United States District Court for the District of Maryland, at Baltimore. Catherine C. Blake, Senior District Judge. (1:18-cv-02013-CCB)

Argued: May 6, 2025 Decided: July 16, 2025

Before HARRIS and QUATTLEBAUM, Circuit Judges, and KEENAN, Senior Circuit Judge.

Affirmed by published opinion. Senior Judge Keenan wrote the opinion, in which Judge Harris and Judge Quattlebaum agreed.

Danielle D. Giroux, HARMAN CLAYTOR CORRIGAN & WELLMAN, Glen Allen, Virginia, for Appellant/Cross-Appellee. Kelly Marie Lippincott, GORDON REES SCULLY MANSUKHANI, LLP, Alexandria, Virginia, for Appellee/Cross-Appellant.

BARBARA MILANO KEENAN, Senior Circuit Judge:

In this appeal, we consider whether the district court erred (1) in awarding summary judgment to Stradis Health Care, LLC (Stradis) on its claim of implied indemnification against a joint tortfeasor, Geri-Care Pharmaceuticals Corporation (Geri-Care), and (2) in denying Stradis’ request that Geri-Care be ordered to pay Stradis’ attorneys’ fees. In a prior appeal involving these parties, we affirmed the district court’s judgment in favor of plaintiff KeraLink International, Inc. (KeraLink), the operator of a national network of “eyebanks,” on its strict products liability claim against Stradis and Geri-Care, two suppliers of contaminated eyewash used to remove donated eye tissue for future transplant. KeraLink Int’l v. Geri-Care Pharm., 60 F.4th 175 (4th Cir. 2023). Stradis and Geri-Care were held jointly and severally liable for the judgment amount of $606,415.49 plus prejudgment interest.

Upon our review, we hold that the district court did not err under Maryland law in awarding Stradis implied indemnification against Geri-Care for the products liability judgment, based on the court’s conclusion that Stradis’ culpability in distribution of the contaminated eyewash product was secondary to Geri-Care’s primary culpability as the apparent manufacturer of the product. We also conclude that the district court did not err or abuse its discretion under Maryland law in denying Stradis’ claim for attorneys’ fees based on the court’s application of the “American Rule,” which ordinarily precludes the recovery of attorneys’ fees as compensatory damages unless authorized by statute, rule, or contract. We therefore affirm the district court’s judgment.

I.

We state the relevant facts as set forth in our prior decision. Id. KeraLink, which maintains its business headquarters in Maryland, operates a network of eyebanks in many states and collects corneas and donated eye tissue for future transplants. KeraLink purchased from Stradis a number of “surgical packs” containing “eyewash,” among other products. Stradis had purchased this eyewash from a third party, which had bought the eyewash from Geri-Care. Geri-Care, in turn, had procured the eyewash from Kareway Product, Inc. (Kareway), which had obtained the eyewash from a Korean manufacturing company.

After receiving the eyewash from Kareway, Geri-Care did not test the eyewash for pathogens but relied on Kareway’s certification that the contents of each box of bottled eyewash were sterile. Geri-Care registered the eyewash with the Food & Drug Administration (FDA) and inspected the bottles’ seals and expiration dates. The label on each eyewash bottle displayed Geri-Care’s logo, stated that the bottle was “distributed by” Geri-Care, and that the eyewash was a “Product of Korea.” Geri-Care listed no other entities on the eyewash labeling.

Before Geri-Care marketed the product, Geri-Care requested that Kareway make changes to the label, including changes to the directions for use, changes to the expiration dates, and the addition of a statement asserting that the contents were comparable to another named brand of eyewash. The Geri-Care eyewash label stated that the eyewash was a “STERILE EYE IRRIGATING SOLUTION.”

When the eyewash arrived at Stradis’ facility in Georgia, each bottle already had been individually sealed. After ensuring that the plastic seal on the cap of each bottle was secure, Stradis placed the eyewash bottles into surgical packs that also contained other items. Stradis included in each surgical pack sent to KeraLink an insert listing the pack’s contents, including “sterile eye wash.” The insert also contained a statement that Stradis had manufactured and distributed the surgical packs.

The Eye Bank Association of America later notified KeraLink about potentially contaminated eyewash. KeraLink confirmed the presence of contaminants in eight of ten bottles tested and identified certain lot numbers of Stradis’ surgical packs containing the potentially contaminated eyewash. Corneal tissue recovered with this contaminated eyewash was rendered unusable. The record showed that testing conducted by Stradis and Geri-Care after the reports of contamination confirmed that the eyewash was contaminated when it left Geri-Care’s and Stradis’ possession.

KeraLink filed suit against Stradis and Geri-Care in the trial court asserting claims for strict products liability and other claims. Stradis filed a third-party complaint against Geri-Care and other entities not involved in this appeal. As relevant here, the district court initially awarded summary judgment to KeraLink on its strict products liability claim against both Geri-Care and Stradis.1

1

KeraLink alleged additional claims against Stradis and Geri-Care. Those claims are not relevant to this appeal. See KeraLink, 60 F.4th at 180 nn.2 & 3.

Neither Stradis nor Geri-Care disputed that KeraLink could prove the elements for a strict products liability claim, but both parties sought to avoid liability by asserting a “sealed container defense.”2 See id. at 181 (setting forth elements of strict products liability under Maryland law: (1) “the product was in [a] defective condition at the time that it left the possession or control of the seller”; (2) the product was “unreasonably dangerous to the user or consumer”; (3) “the defect was a cause of the injuries”; and (4) “the product was expected to and did reach the consumer without substantial change in its condition” (quoting Phipps v. Gen. Motors Corp., 363 A.2d 955, 958 (Md. 1976))). The district court rejected Stradis’ and Geri-Care’s affirmative defenses and entered “final judgment” on KeraLink’s claims against Stradis and Geri-Care under Federal Rule of Civil Procedure 54(b), thus permitting Stradis and Geri-Care to appeal to this Court. In its judgment, the district court held that Stradis and Geri-Care were jointly and severally liable to pay KeraLink $606,415.49, plus prejudgment interest. Notably, KeraLink did not seek and was not awarded any attorneys’ fees from Stradis or Geri-Care.

On appeal, we affirmed this part of the district court’s judgment. Id. at 188. In our analysis, we agreed with the district court that Geri-Care was barred under Maryland Code, Cts. & Jud. Proc. § 5-405(b) from asserting a “sealed container defense” to the products liability claim, because Geri-Care had held “itself out as a manufacturer.” Id. at 182-83. We explained that there was no basis on which a purchaser, sophisticated or otherwise,

2

Geri-Care also asserted an affirmative defense based on the “economic loss rule.”

We affirmed the district court’s analysis that Geri-Care was not entitled to rely on this rule. Id. at 184-86.

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