Data Foundry

Medical device recalls 2025

Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Model/Catalog… — Class II medical device recall Z-2512-2025

Ongoing recall by Integra LifeSciences Corp. (NeuroSciences), reported 2025-09-10, distributed nationwide. Packaging failures were identified which could lead to a breach in the sterile barrier.

Recall numberZ-2512-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmIntegra LifeSciences Corp. (NeuroSciences), Princeton, NJ, United States
Recall initiated2025-08-05
Classified2025-09-03
Reported by FDA2025-09-10
DistributedNationwide (US)
Countries outside the USAU, CA, KR, MY, NZ
Quantity111,492 units
Reason classessterility, packaging
UPC / GTIN / UDI-DI00050428462584, 00050428510377
Lot numbers014524, 014622, 020124, 020923, 040923, 044622, 054623
Model numbers9370613, 937404, CVS9370613, CVS937404

Product

Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Model/Catalog Number: 9370613, 937404 Product Description: Infused with natural medical-grade honey Manuka (Leptospermum) honey is a medical-grade honey that is harvested from bees in New Zealand. Researchers have found that this species has unique components that make it ideal for wounds.

Reason for recall

Packaging failures were identified which could lead to a breach in the sterile barrier.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2512-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.