ClearanceBrief
Recall Z-0392-2022 ยท HRS Plate, Fixation, Bone

Wright Medical Technology Inc

Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.

DateDec 3, 2021
StatusOpen, Classified
ReasonThe incorrect product is contained in the packaging.
Root causeUnder Investigation by firm
ActionThe recalling firm issued a recall letter dated 03 Dec 2021 on 12/3/2021 via Fed Ex Priority Overnight. The letter explained the packages labeled as the CLAW II 4 Hole Plates and the packages labeled as the DARCO Locking Screws were switched, resulting in the packages containing the incorrect product. The letter also provided the potential risks, the actions needed to be taken, and provided example labels of affected products. The consignee is to immediately check their inventory to locate the packaged product and remove them from their point of use. The enclosed business reply form was to
Quantity23 units
DistributionWorldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K113014CLAW II POLYAXIAL COMPRESSION SYSTEM AND ORTHOLOC 3DSI LOCKING SCREWS
Wrightmedicaltechnologyinc, Jan 31, 2012