FDA Device recall Z-1676-2016
Periarticular plating system, cancellous bone screw, partially threaded, hex head, 4.0 mm diameter, 16 mm length 47234702116
- FDA Device
- Class II
- terminated
- Published 2016-05-25
On 2016-05-25 the FDA classified a Class II recall of Periarticular plating system, cancellous bone screw, partially threaded, hex head, 4.0 mm diameter, 16 mm length 47234702116 by Zimmer Manufacturing B V, citing A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1676-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-05-04 |
| Published | 2016-05-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Manufacturing B V |
| Distribution | US |
Product
Periarticular plating system, cancellous bone screw, partially threaded, hex head, 4.0 mm diameter, 16 mm length 47234702116
Reason
A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
Identifiers
| code_info | LOT: 63146423 |
|---|
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-1676-2016%22
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