Data Foundry

Medical device recalls 2025

Brand Name: Wolf-Pak Product Name: Dressing Change Kit with… — Class II medical device recall Z-1013-2025

Ongoing recall by Trinity Sterile, Inc., reported 2025-01-29, distributed nationwide. Potential for hole in package compromising sterility of the medical kit.

Recall numberZ-1013-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmTrinity Sterile, Inc., Salisbury, MD, United States
Recall initiated2024-12-13
Classified2025-01-22
Reported by FDA2025-01-29
DistributedNationwide (US)
Quantity1,980 units
Reason classessterility
UPC / GTIN / UDI-DI10857800006841
Lot numbers600018
Model numbersDC3077LF

Product

Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Transparent Dressing & 3mL CHG One Step Applicator CS/30 Model/Catalog Number: DC3077LF Software Version: N/A Product Description: Dressing change kit, case of 30, lot #600018, 66 cases affected. Component: No

Reason for recall

Potential for hole in package compromising sterility of the medical kit.

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-1013-2025. 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.