FDA Device recall Z-0953-2021
Ethicon Dermabond Advanced Topical Skin Adhesive-topical skin adhesive to hold closed easily approximated skin edges of wounds from surgica…
- FDA Device
- Class II
- terminated
- Published 2021-02-10
On 2021-02-10 the FDA classified a Class II recall of Ethicon Dermabond Advanced Topical Skin Adhesive-topical skin adhesive to hold closed easily approximated skin edges of wounds from surgica… by Ethicon, citing product distributed with a red tape as part of the sterile packaging which could impact the seal and result in a sterility breach.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0953-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-01-04 |
| Published | 2021-02-10 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ethicon |
| Distribution | US |
Product
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
Product distributed with a red tape as part of the sterile packaging which could impact the seal and result in a sterility breach
Identifiers
| code_info | Lot Number: QEBBTQ Exp. Date: April 30, 2022 GTIN: 10705031203532 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0953-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.