FDA recall record

INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup recall — FDA Z-1753-2024

54 MM finisher blade was inadvertently affixed to the shaft of the CupX handle in lieu of the 54 MM starter blade.

Class IIclassification
Z-1753-2024official record ID
May 8, 2024report date

Recall record at a glance

Official recordZ-1753-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusCompleted
Recalling firmInnomed, Inc.
Report dateMay 8, 2024
Recall initiation dateMar 7, 2024
Quantity41 devices
LocationSavannah, GA, United States

Official product description

INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup

Why the product was recalled

54 MM finisher blade was inadvertently affixed to the shaft of the CupX handle in lieu of the 54 MM starter blade.

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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