1 — Class II medical device recall Z-1220-2017
Terminated recall by Zimmer Biomet, Inc., reported 2017-02-22. The identification of the devices was non-conforming with off-centered slots and the no-go gage starting in th
| Recall number | Z-1220-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2017-01-10 |
| Classified | 2017-02-16 |
| Reported by FDA | 2017-02-22 |
| Terminated | 2018-03-26 |
| Countries outside the US | JP |
| Quantity | 11 |
| Lot numbers | 1.5X4MMHT |
| Model numbers | 530430 |
Product
1.5mm System, Cranio-maxillofacial Bone Screws 1.5 x 4mm HT SD X-DR Screw, Bone Screw
Reason for recall
The identification of the devices was non-conforming with off-centered slots and the no-go gage starting in the pilot hole.
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-1220-2017. 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.