Class II — Innomed, Inc.
| Recalling firm | INNOMED, INC. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Completed |
| Reason | 54 MM finisher blade was inadvertently affixed to the shaft of the CupX handle in lieu of the 54 MM starter blade. |
| Product | INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup |
| Quantity | 41 devices |
| Distribution | FL, GA, PA, NY, CA, VA, SD, MN, TX, UT, NC, and UK, Denmark, Germany Switzerland, Ireland, Canada |
| Initiated | 2024-03-07 |
| Classified | 2024-05-01 |
| Recall number | Z-1753-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Innomed, Inc. (Z-1753-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94337/
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