FDA Recall Terminated

T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits (GWK 300) - Product Usage: Intended to be used to insert screws with T25 driving features, which includes screws with diameters of 5.5mm, 6.5mm, and 7.3mm Product Code: GWK 300

Recall: Z-1698-2021 · Initiated April 15, 2021

Recall

Recall Number
Z-1698-2021
Event Number
87906
Firm
Flower Orthopedics Corporation
FEI Number
3009996260
Product Code
HXX
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
April 15, 2021
Terminated
November 12, 2021
Address
100 Witmer Rd, Ste 280, Horsham, PA, 19044-2647

Description

T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits (GWK 300) - Product Usage: Intended to be used to insert screws with T25 driving features, which includes screws with diameters of 5.5mm, 6.5mm, and 7.3mm Product Code: GWK 300

Reason

Cannulated Screwdrivers may break at the driver tip along the shaft, near the handle extending surgery time and additional x-ray to identify the fragments from the breakages

Action

Flower Orthopedic issued Urgent Recall Information via email on 4/15/21. Letter states reason for recall, health risk and action to take: Check your inventory for the product listed below and quarantine immediately. Next, please complete and return the attached Acknowledgement and Receipt Form as soon as possible. Flower Orthopedics is initiating shipment of replacement product for delivery Friday April 16. Contact information for questions: Monday through Friday, 8:30 AM to 5:00 PM, EDST 877-778-8587 or [email protected] "Acknowledgement and Product Replacement Forms (see attached)

Distribution

US Nationwide distribution in the states of AZ, CO, FL, GA, IL, IN, PA, NC, VA.

Quantity

47 units