RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High… — Class II medical device recall Z-1024-2017
Terminated recall by Zimmer Biomet, Inc., reported 2017-01-25, distributed nationwide. Product complaints indicated that the part and lot numbers on the packaging differed from the physical product
| Recall number | Z-1024-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2016-12-19 |
| Classified | 2017-01-13 |
| Reported by FDA | 2017-01-25 |
| Terminated | 2017-09-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR |
| Quantity | 36 |
| UPC / GTIN / UDI-DI | 00880304651494, 00880304651524 |
| Lot numbers | 419460, 761680 |
| Model numbers | XL-108223, XL-108323 |
Product
RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item XL-108323 ArComXL MaxRom +3mm Liners Size 23 item XL-108223
Reason for recall
Product complaints indicated that the part and lot numbers on the packaging differed from the physical product inside the packaging. Risk of delay in surgery.
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-1024-2017. 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.