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Smith & Nephew, Inc. recalls CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Usage: used for interference fixation of bone-tendon-bone of s
Recalled May 5, 2021 · FDA recall Z-1510-2021 · Smith & Nephew
Hazard
Mislabeled box contained a 6mm x 20mm screw instead of 6mm x 30mm screw · FDA Class II
Units
2 units US and 193 units OUS. 195 units WW
Sold at
Worldwide distribution - US Nationwide distribution in the state of FL and the countries of Australia, Japan.
Description
Mislabeled box contained a 6mm x 20mm screw instead of 6mm x 30mm screw
Product
CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Usage: used for interference fixation of bone-tendon-bone of soft tissue grafts in anterior cruciate ligament reconstruction, Part Number: 014208
Manufacturer(s)
Smith & Nephew, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →