G7 Acetabular System — Class II medical device recall Z-0007-2023
Ongoing recall by Zimmer, Inc., reported 2022-10-12, distributed nationwide. The outer sterile package cavity has a corner wall thickness that is below the specification. The thin corner
| Recall number | Z-0007-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2022-08-25 |
| Classified | 2022-10-05 |
| Reported by FDA | 2022-10-12 |
| Distributed | Nationwide (US) |
| Quantity | 56 us |
| Reason classes | sterility, packaging |
| UPC / GTIN / UDI-DI | 00880304524224, 00880304524262 |
| Lot numbers | 7253325, 7286477, 7289929, 7296576, 7296633, 7301697 |
| Model numbers | 010000663, 010000667 |
| Expiration dates | 2032-06-13, 2032-07-21 |
Product
G7 Acetabular System, Acetabular Shell, Item numbers Item Numbers: 010000663 (52 MM E), 010000667 (60 MM G). used in hip arthroplasty
Reason for recall
The outer sterile package cavity has a corner wall thickness that is below the specification. The thin corner wall could potentially crack during transit. Potential risks include non-clinically or clinically significant extension of surgery, or infection leading to surgical intervention.
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-0007-2023. 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.