FDA Recall Terminated

Kinamed SuperCable Grip and Plate System Driver, 3.5mm Hex, Catalog Number: 35-860-2060 The driver is intended to be used in conjunction with compression and locking bone screws for fixation of long bone fractures when Kinamed Trochanteric Grips & Cable-Plates are used. Subsequent Product Codes: HWC, JDQ.

Recall: Z-2588-2011 · Initiated August 18, 2010

Recall

Recall Number
Z-2588-2011
Event Number
58808
Firm
Kinamed Inc
FEI Number
2027148
Product Code
KTT
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
August 18, 2010
Posted
June 17, 2011
Terminated
October 25, 2011
Address
820 Flynn Rd, Camarillo, CA, 93012

Description

Kinamed SuperCable Grip and Plate System Driver, 3.5mm Hex, Catalog Number: 35-860-2060 The driver is intended to be used in conjunction with compression and locking bone screws for fixation of long bone fractures when Kinamed Trochanteric Grips & Cable-Plates are used. Subsequent Product Codes: HWC, JDQ.

Reason

The recall was initiated due to inadequate mechanical strength of these screwdrivers' hexagonal tip feature, causing it to strip during final tightening.

Action

The firm, Kinamed Inc., sent a recall letter dated August 18, 2010 to consignees/customers via FedEx. The letter described the product, problem and actions to be taken. The customers were instructed to Immediately examine their stock and return any Kinamed SuperCable Screwdriver, 3.5mm Hex bearing these lot numbers, along with the completed attached Effectiveness Check Form and shipment under RMA #74567 to the attention of: "Director of Quality Assurance" Kinamed, Inc. 820 Flynn Road Carnarillo, CA 93012-8701 Note: The Kinamed sales agent shipped and had the product replaced for the customers. If you have any questions, please contact (303)-681-2208, (805) 384-2748 or (800) 827-5775

Distribution

Worldwide distribution: USA (nationwide) state of: CO and country of: Columbia.

Quantity

8 units