FDA Device recall Z-2602-2018
Zimmer Dermatone AN, Model No. 88710100
- FDA Device
- Class II
- terminated
- Published 2018-08-08
On 2018-08-08 the FDA classified a Class II recall of Zimmer Dermatone AN, Model No. 88710100 by Zimmer Surgical, citing devices may have a loose control bar, which could compromise the ability to control the thickness of the graft. Devices could also have a loose width plate that if undetected, cou….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2602-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-08 |
| Published | 2018-08-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Surgical |
| Distribution | AL, AZ, CA, FL, IA, IL, MA, MI, MN, MS, NH, NJ, NY, OH, RI, SD, TX |
Product
Zimmer Dermatone AN, Model No. 88710100
Reason
Devices may have a loose control bar, which could compromise the ability to control the thickness of the graft. Devices could also have a loose width plate that if undetected, could result in an imperfect, yet still usable graft. Potential risks include harvesting a skin graft of a thickness much greater than intended, described as patient gouged, minor delay of surgery, and sub-optimal (but usable) graft.
Identifiers
| code_info | Lots 63578134 , 63578135, 63592351, 63618116, 63646910, 63817639, 63898373 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2602-2018%22
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