FDA Recall Open, Classified

EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007.

Recall: Z-0479-2021 · Initiated June 19, 2020

Recall

Recall Number
Z-0479-2021
Event Number
85943
FEI Number
1000116912
Product Code
HSX
Status
Open, Classified
Root Cause
Other
Initiated
June 19, 2020
Address
9800 Metric Blvd, Encore Medical, LP, Austin, TX, 78758-5445

Description

EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007.

Reason

There have been issues experienced with the peg preparation steps, specifically drilling of the Femoral posterior peg. Upon drilling, the shaft portion of the drill may bind within the Posterior Peg drill guide. The extended length of the drill guide and tight tolerances to ensure accurate preparation seem to be contributing to this situation. There is a potential of a delay in surgery if this issue were to recur.

Action

The method of notification was via e-mail to surgical sales agents, and the notices were issued on 06/18/2020. Additionally, a notification to return the affected drills for replacement were sent via e-mail to affected surgical agents on 07/20/20. The following recommendations should be communicated to the implanting surgeons: Sales Agents Action: To avoid the potential binding, the following is recommended: " Use a plunge mill approach, i.e. plunge the drill in and out of the drill guide bushing a few times slowly until the hole is fully prepared. " Use of saline or fat to keep the drill lubricated during use. " Inspect all instrumentation prior to use to identify any wear, breakage or damage. Along with the notification, the communication includes an acknowledgment form that should be completed and returned to confirm that the instructions provided have been read and understood. THE ACKNOWLEDGEMENT SHOULD BE REVIEWED AND COMPLETED BY JULY 6, 2020.For questions, contact Teffany Hutto by phone at (512) 834-6255 or by email at [email protected].

Distribution

US: AZ, CA, FL, GA, IL, IN, MI, MN, NY, TX, VA, and WA.. No OUS Consignees.

Quantity

28 units