U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
The recall was initiated due to inadequate mechanical strength of these screwdrivers' hexagonal tip
feature, causing it to strip during final tightening.
조치
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
Worldwide distribution: USA (nationwide) state of: CO and country of: Columbia.
제품 설명
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.