FDA Device recall Z-2110-2017
Brennen Skin Graft Mesher
- FDA Device
- Class II
- ongoing
- Published 2017-05-24
On 2017-05-24 the FDA classified a Class II recall of Brennen Skin Graft Mesher by Molnlycke Health Care, citing sterilization validation failure.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2110-2017 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-04-24 |
| Published | 2017-05-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Molnlycke Health Care |
| Distribution | US |
Product
Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'
Reason
Sterilization validation failure.
Identifiers
| code_info | Code: 131600, 131601, 131602, 131603, 131604, 131500, 131501, 131502, 131503, 131504 and 131506. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2110-2017%22
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