HipLOC CHS Plate/Lag Screw Introducer — Class II medical device recall Z-0885-2016
Terminated recall by Biomet, Inc., reported 2016-03-02, distributed in AZ, GA, IL, KY, MI, MN, MO, NC…. A complaint was received where the Hiploc Plate/Lag Screw Introducer was undersized and would not accept the i
| Recall number | Z-0885-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2016-02-16 |
| Classified | 2016-02-25 |
| Reported by FDA | 2016-03-02 |
| Terminated | 2017-02-14 |
| Distributed | AZ, GA, IL, KY, MI, MN, MO, NC, NJ, PA, UT |
| Countries outside the US | NL |
| Quantity | 23 units |
| Model numbers | 35-000263 |
Product
HipLOC CHS Plate/Lag Screw Introducer
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0885-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.