PlainRecalls
FDA Devices Moderate Class II Terminated

Ethicon Dermabond Advanced Topical Skin Adhesive-topical skin adhesive to hold closed easily approximated skin edges of wounds from surgical incisions, including incisions Product Code: DNX12

Reported: February 10, 2021 Initiated: January 4, 2021 #Z-0953-2021

Product Description

Ethicon Dermabond Advanced Topical Skin Adhesive-topical skin adhesive to hold closed easily approximated skin edges of wounds from surgical incisions, including incisions Product Code: DNX12

Reason for Recall

Product distributed with a red tape as part of the sterile packaging which could impact the seal and result in a sterility breach

Details

Recalling Firm
Ethicon, Inc.
Units Affected
23,580 eaches
Distribution
US Nationwide
Location
Somerville, NJ

Frequently Asked Questions

What product was recalled?
Ethicon Dermabond Advanced Topical Skin Adhesive-topical skin adhesive to hold closed easily approximated skin edges of wounds from surgical incisions, including incisions Product Code: DNX12. Recalled by Ethicon, Inc.. Units affected: 23,580 eaches.
Why was this product recalled?
Product distributed with a red tape as part of the sterile packaging which could impact the seal and result in a sterility breach
Which agency issued this recall?
This recall was issued by the FDA Devices on February 10, 2021. Severity: Moderate. Recall number: Z-0953-2021.