FDA recall record

Encore Medical Empowr PS Knee Tibial Insert recall — FDA Z-1139-2017

The Empowr PS Insert was reported as missing the impaction slot feature.

Class IIclassification
Z-1139-2017official record ID
Feb 15, 2017report date

Recall record at a glance

Official recordZ-1139-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEncore Medical, Lp
Report dateFeb 15, 2017
Recall initiation dateJan 10, 2017
Quantity24 units
LocationAustin, TX, United States

Official product description

Empowr PS Knee Tibial Insert; Model 343-14-709 The EMPOWR PS tibial insert are made from Highly Cross-Linked Vitamin E (HXL VE) UHMWPE. The tibial insert implants are intended to mate with tibial base implants.

Why the product was recalled

The Empowr PS Insert was reported as missing the impaction slot feature.

Distribution information

Nationwide Distribution to CO, NY, and FL

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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