CARROLLTON HIP FX Convenience kit used for surgical procedures — Class II medical device recall Z-0349-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-11-20, distributed nationwide. Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on
| Recall number | Z-0349-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2024-10-04 |
| Classified | 2024-11-08 |
| Reported by FDA | 2024-11-20 |
| Distributed | Nationwide (US) |
| Quantity | 36 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 10889942848447 |
| Lot numbers | 24EBP466 |
Product
CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A
Reason for recall
Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.
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-0349-2025. 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.