FDA Device recall Z-2336-2016
Zimmer¿ Air Dermatome II Width Plate, 1 in., item number 00-8851-201-00 . Width plates is packaged inside of a padded-foam corrugate box
- FDA Device
- Class II
- terminated
- Published 2016-08-10
On 2016-08-10 the FDA classified a Class II recall of Zimmer¿ Air Dermatome II Width Plate, 1 in., item number 00-8851-201-00 . Width plates is packaged inside of a padded-foam corrugate box by Zimmer Surgical, citing the surface coating applied to the device is blistering, peeling and discoloring after usage over time.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2336-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-07-04 |
| Published | 2016-08-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Surgical |
| Distribution | US |
Product
Zimmer¿ Air Dermatome II Width Plate, 1 in., item number 00-8851-201-00 . Width plates is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or padded envelope. The Zimmer Air Dermatome II is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities.
Reason
The surface coating applied to the device is blistering, peeling and discoloring after usage over time
Identifiers
| code_info | Lot # 61999883, Serial # N/A Lot # 62243337, Serial # N/A Lot # 62282028, Serial # N/A Lot # 62393990, Serial # N/A |
|---|
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-2336-2016%22
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