FDA Recall Open, Classified

SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit, Product No. SE-2020-10. Used with DePuy Synthes SPEEDSHIFT Continuous Compression Staple Implants for bone fixation and management of fracture and reconstructive surgery.

Recall: Z-0098-2023 · Initiated September 27, 2022

Recall

Recall Number
Z-0098-2023
Event Number
90918
Firm
Synthes (USA) Products LLC
FEI Number
3008812560
Product Code
JDR
Status
Open, Classified
Root Cause
Error in labeling
Initiated
September 27, 2022
Posted
October 18, 2022
Address
1301 Goshen Pkwy, West Chester, PA, 19380-5986

Description

SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit, Product No. SE-2020-10. Used with DePuy Synthes SPEEDSHIFT Continuous Compression Staple Implants for bone fixation and management of fracture and reconstructive surgery.

Reason

The subject products are being recalled because they contain the incorrect size drill guide and will not prepare the bone correctly for the size of the implant included in the sterile kit. If the incorrect drill guide is used, there is potential for bone damage due to incorrectly placed drill holes for the implant included in the kit.

Action

On September 27, 2022, the firm notified affected customers via urgent medical Device Recall letters. Customers were instructed to examine their inventory to determine if they have affected product and to quarantine them immediately - Customers should not use the recalled products. Customers should contact their DePuy Synthes Sales Consultant or call the customer support services at [email protected] to coordinate the return/credits of the subject products.

Distribution

US Nationwide distribution.

Quantity

81