Smith & Nephew, Inc. recalls
17 federal recalls on file, showing the 3 from the last 12 months. We read every CPSC, FDA, USDA and NHTSA notice for Smith & Nephew, Inc. and put it in plain English.
Recent recalls
Smith & Nephew EVOS tibia plate recalled for mislabelingSmith & Nephew recalled seven units of the EVOS 3.5MM Lateral Proximal Tibia Plate, 6 Hole Left, 91MM. The implants were labeled and laser etched as a standard lateral tibia plate, but they are actually a partial articular version. No injuries have been reported.
ModerateFDAOct 30, 2026
- Smith & Nephew TRIGEN humeral nail recalled for manufacturing defect
Smith & Nephew identified a manufacturing error in certain TRIGEN Proximal Straight Humeral Nails (8/7 X 16, Ref: 71760816) in which the distal holes are missing. If implanted without detection, the affected nail could require revision surgery. Five units were distributed internationally.
ModerateFDAJun 24, 2026
- Check Smith & Nephew bone screws for labeling error
Smith & Nephew is recalling certain BIOSURE HA Screws (6mm x 20mm bone fixation screws) due to a labeling error on affected units. The screws themselves are safe, but the packaging labels on a small number of units contain incorrect information. No injuries have been reported.
ModerateFDADec 24, 2025