G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip… — Class II medical device recall Z-0626-2018
Terminated recall by Zimmer Biomet, Inc., reported 2018-02-21, distributed nationwide. The affected products are labeled and etched as F-44 mm liners; however, the physical products could potential
| Recall number | Z-0626-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2017-08-25 |
| Classified | 2018-02-15 |
| Reported by FDA | 2018-02-21 |
| Terminated | 2018-08-16 |
| Distributed | Nationwide (US) |
| Quantity | 8 |
| Reason classes | labeling |
| Lot numbers | 478340 |
| Model numbers | 110024464 |
Product
G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and tissues to be replaced with artificial prosthesis. The result of the procedure is to relieve pain and restore a sense of normal function and mobility to the damaged joint.
Reason for recall
The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.
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-0626-2018. 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.