Smith & Nephew, Inc.: Medical Device Recalls in 2022

Updated on March 25, 2026.

According to to data from the FDA, there were 3 medical device recalls made by Smith & Nephew, Inc. in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND
Acufex Access Advanced Positioning Kit - indicated for use to position and distract the extremity of patient during open and arthroscopic surgical procedures Product Number: 72205104
(1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186. (2) Genesis II Non-Porous Tibial Baseplate Size 4 Left, Product #71420166.