FDA Device recall Z-1753-2024
INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup
- FDA Device
- Class II
- completed
- Published 2024-05-08
On 2024-05-08 the FDA classified a Class II recall of INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup by Innomed, citing 54 MM finisher blade was inadvertently affixed to the shaft of the CupX handle in lieu of the 54 MM starter blade.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1753-2024 |
| Classification | Class II |
| Status | completed |
| Initiated | 2024-03-07 |
| Published | 2024-05-08 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Innomed |
| Distribution | CA, FL, GA, MN, NC, NY, PA, SD, TX, UT, VA |
Product
INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup
Reason
54 MM finisher blade was inadvertently affixed to the shaft of the CupX handle in lieu of the 54 MM starter blade.
Identifiers
| code_info | UDI/DI 00840277104007, Lot Number 1223K |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1753-2024%22
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