FDA recall record

Encore Medical RSP Impaction Fixture recall — FDA Z-1413-2017

During the Turon assembly, the impaction forces caused the polymer, black acetal copolymer from the Impaction Fixture to wear off on the lateral surface…

Class IIclassification
Z-1413-2017official record ID
Mar 15, 2017report date

Recall record at a glance

Official recordZ-1413-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEncore Medical, Lp
Report dateMar 15, 2017
Recall initiation dateFeb 9, 2017
Quantity626 units
LocationAustin, TX, United States

Official product description

RSP Impaction Fixture

Why the product was recalled

During the Turon assembly, the impaction forces caused the polymer, black acetal copolymer from the Impaction Fixture to wear off on the lateral surface of the Humeral Stem titanium plasma spray coating.

Distribution information

US, South Korea, Australia, Canada, United Kingdom/Ireland, Germany

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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