INNOMED CUP REMOVAL STARTER INSTRUMENT — Class II medical device recall Z-1753-2024
Completed recall by Innomed, Inc., reported 2024-05-08, distributed in CA, FL, GA, MN, NC, NY, PA, SD…. 54 MM finisher blade was inadvertently affixed to the shaft of the CupX handle in lieu of the 54 MM starter bl
| Recall number | Z-1753-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Innomed, Inc., Savannah, GA, United States |
| Recall initiated | 2024-03-07 |
| Classified | 2024-05-01 |
| Reported by FDA | 2024-05-08 |
| Distributed | CA, FL, GA, MN, NC, NY, PA, SD, TX, UT, VA |
| Countries outside the US | CA, CH, DE, DK, GB, IE |
| Quantity | 41 devices |
| UPC / GTIN / UDI-DI | 00840277104007 |
| Lot numbers | 1223K |
| Model numbers | 520054 |
Product
INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup
Reason for recall
54 MM finisher blade was inadvertently affixed to the shaft of the CupX handle in lieu of the 54 MM starter blade.
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-1753-2024. 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.