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Stryker Howmedica Osteonics Corp. recalls Stryker 1) Asnis III Cannulated Screw REF 604640 4.0x40mm TL 13.5mm 2) Asnis III Cannulated Screw REF 604642S 4.0
Recalled September 4, 2013 · FDA recall Z-2099-2013 · Stryker Howmedica Osteonics
Hazard
Stryker received a report that the length of the cannulated screw asnis III, article # 604640 Lot R11482, was incorrect. · FDA Class II
Units
23 units
Sold at
USA Nationwide Distribution in the states of: FL. OH, TX, & VA
Description
Stryker received a report that the length of the cannulated screw asnis III, article # 604640 Lot R11482, was incorrect.
Product
Stryker 1) Asnis III Cannulated Screw REF 604640 4.0x40mm TL 13.5mm 2) Asnis III Cannulated Screw REF 604642S 4.0x42mm TL 14mm, sterile Product Usage: The Asnis III Cannulated Screw System is intended for fracture fixation of small and long bones and of the pelvis. The system is not intended for spinal use.
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →