PlainRecalls
FDA Devices Moderate Class II Terminated

EMPOWR Porous Knee System TIBIAL PUNCH, SMALL, REF 801-05-202, NON STERILE, Qty 1 For use in orthopedic surgery.

Reported: January 17, 2018 Initiated: December 12, 2017 #Z-0327-2018

Product Description

EMPOWR Porous Knee System TIBIAL PUNCH, SMALL, REF 801-05-202, NON STERILE, Qty 1 For use in orthopedic surgery.

Reason for Recall

The Locking Punch Guide was not sufficiently guiding the large press fit punch, causing the implant to be placed 2-3mm more posterior than intended.

Details

Recalling Firm
Encore Medical, Lp
Units Affected
2 units
Distribution
One medical device distributor in California.
Location
Austin, TX

Frequently Asked Questions

What product was recalled?
EMPOWR Porous Knee System TIBIAL PUNCH, SMALL, REF 801-05-202, NON STERILE, Qty 1 For use in orthopedic surgery.. Recalled by Encore Medical, Lp. Units affected: 2 units.
Why was this product recalled?
The Locking Punch Guide was not sufficiently guiding the large press fit punch, causing the implant to be placed 2-3mm more posterior than intended.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 17, 2018. Severity: Moderate. Recall number: Z-0327-2018.