Recall Z-1013-2025— Trinity Sterile, Inc.

Class II · Ongoing

Class II FDA medical device recall by Trinity Sterile, Inc., initiated 2024-12-13. FDA's recall record names no specific 510(k) clearance for this event. 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: Potential for hole in package compromising sterility of the medical kit..

Recalling firm
Trinity Sterile, Inc.
Classification
Class II
Status
Ongoing
Initiated
2024-12-13
Firm location
Salisbury, MD, United States

Product description

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.