FDA recall record

Encore Medical Exprt Precision System: Revision Knee, Model Number 160-010-726/738 For use recall — FDA Z-0165-2016

The labeling is missing the size/diameter information.

Class IIclassification
Z-0165-2016official record ID
Nov 4, 2015report date

Recall record at a glance

Official recordZ-0165-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEncore Medical, Lp
Report dateNov 4, 2015
Recall initiation dateSep 16, 2015
Quantity209 units
LocationAustin, TX, United States

Official product description

Exprt Precision System: Revision Knee, Model Number 160-010-726/738 For use with the Exprt Knee System in total knee arthroplasty to replace the native patella.

Why the product was recalled

The labeling is missing the size/diameter information.

Distribution information

US Distribution to the states of : SC, WI, RI, NY, MO, AR, OK, GA, FL, AL, CA, AZ and CO.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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