FDA Device recall Z-2918-2016
Arthrex Suture Washer
- FDA Device
- Class III
- terminated
- Published 2016-10-12
On 2016-10-12 the FDA classified a Class III recall of Arthrex Suture Washer by Arthrex, citing the device was assembled incorrectly. Suture and washer were not assembled; components were placed loose in the package.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2918-2016 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-08-12 |
| Published | 2016-10-12 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Arthrex |
| Distribution | CA, CO, FL, ID, KY, MA, MN, NY, OR |
Product
Arthrex Suture Washer
Reason
The device was assembled incorrectly. Suture and washer were not assembled; components were placed loose in the package.
Identifiers
| code_info | Unique Device Identifier (UDI): 00888867118607; Catalog # AR-7000-18T; Batch #10028617. |
|---|
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-2918-2016%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.