PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: November 15, 2023 Initiated: September 29, 2023 #Z-0258-2024

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Encore Medical, LP
Units Affected
406
Distribution
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
Location
Austin, TX

Frequently Asked Questions

What product was recalled?
DJO EMPOWR Knee Punch Handle, REF: 801-05-040. Recalled by Encore Medical, LP. Units affected: 406.
Why was this product recalled?
Knee punch handle tip is breaking during surgery due to the lack of heat treatment, which may lead to a disruption in surgery.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 15, 2023. Severity: Moderate. Recall number: Z-0258-2024.