FDA Device recall Z-0885-2016
HipLOC CHS Plate/Lag Screw Introducer
- FDA Device
- Class II
- terminated
- Published 2016-03-02
On 2016-03-02 the FDA classified a Class II recall of HipLOC CHS Plate/Lag Screw Introducer by Biomet, citing A complaint was received where the Hiploc Plate/Lag Screw Introducer was undersized and would not accept the introducor coupling screw. It appears now that not all parts manufactu….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0885-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-02-16 |
| Published | 2016-03-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Biomet |
| Distribution | AZ, GA, IL, KY, MI, MN, MO, NC, NJ, PA, UT |
Product
HipLOC CHS Plate/Lag Screw Introducer
Reason
A complaint was received where the Hiploc Plate/Lag Screw Introducer was undersized and would not accept the introducor coupling screw. It appears now that not all parts manufactured to Rev A drawing were reworked.
Identifiers
| code_info | Catalog Number: 35-000263; and Lot Number Identification: 1807188, 1807189, 1943563, and 2577847. |
|---|
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-0885-2016%22
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