Data Foundry

Medical device recalls 2025

Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog… — Class II medical device recall Z-2505-2025

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-2505-2025
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
Quantity15,441 units
Reason classessterility, packaging
UPC / GTIN / UDI-DI10381780486930
Lot numbers2150, 2151, 2201, 2209, 2217, 2232, 2241, 2301, 2312, 2313, 2314, 2328, 2336, 2337, 2414, 2415, 2417, 2428, 2434, 2435, 2505, 2508, 2509
Model numbers31505

Product

Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿ Paste with Active Leptospermum Honey is a moist dressing made of 100% Active Leptospermum medical grade Honey. The dressing helps maintain a moist environment conducive to wound healing and helps aid and support autolytic debridement. The dressing can be removed without causing trauma to the wound when a primary dressing is used.

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-2505-2025. 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.