# FDA recall Z-1753-2024

> **Innomed, Inc.** · Class II · device recall initiated 2024-03-07.

## 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.

## Distribution

FL, GA, PA, NY, CA, VA, SD, MN, TX, UT, NC, and UK, Denmark, Germany Switzerland, Ireland, Canada

## Key facts

- **Recall number:** Z-1753-2024
- **Recalling firm:** Innomed, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2024-03-07
- **Report date:** 2024-05-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Savannah, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1753-2024

## Citation

> AI Analytics. FDA recall Z-1753-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1753-2024. Source: US FDA. Licensed CC0.

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