FDA recall record

Encore Medical DJO EMPOWR Knee Punch Handle, REF: 801-05-040 recall — FDA Z-0258-2024

Knee punch handle tip is breaking during surgery due to the lack of heat treatment, which may lead to a disruption in surgery.

Class IIclassification
Z-0258-2024official record ID
Nov 15, 2023report date

Recall record at a glance

Official recordZ-0258-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmEncore Medical, LP
Report dateNov 15, 2023
Recall initiation dateSep 29, 2023
Quantity406
LocationAustin, TX, United States

Official product description

DJO EMPOWR Knee Punch Handle, REF: 801-05-040

Why the product was recalled

Knee punch handle tip is breaking during surgery due to the lack of heat treatment, which may lead to a disruption in surgery.

Distribution information

US: VA, TN, MN, TX, IL, IN, KY, OH, SC, MS, RI, ME, NJ, NY, MD, CA, KS, LA, PR, AL, FL, GA, AZ, WA

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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