Class II

Medical Device Recall: INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup

Innomed, Inc. · March 7, 2024

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

States Affected

CA, FL, GA, MN, NC, NY, PA, SD, TX, UT, VA

Quantity Affected

41 devices

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1753-2024

Status: completed

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Innomed, Inc. Medical Device Recall: INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup | SafeCheck