FDA recall record

Encore Medical RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204 recall — FDA Z-0532-2024

Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver

Class IIclassification
Z-0532-2024official record ID
Dec 20, 2023report date

Recall record at a glance

Official recordZ-0532-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmEncore Medical, LP
Report dateDec 20, 2023
Recall initiation dateSep 6, 2023
Quantity146 units
LocationAustin, TX, United States

Official product description

RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.

Why the product was recalled

Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver

Distribution information

U.S.: AZ, CA, FL, IN, KS, KY, ME, MN, MS, NJ, OH, Puerto Rico, RI, SC, TN, TX, VA, and WA O.U.S.: None

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: Letter.

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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