Stryker Instruments Div. of Stryker Corporation: Medical Device Recalls in 2022

According to to data from the FDA, there were 3 medical device recalls made by Stryker Instruments Div. of Stryker Corporation in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

• SurgiCount+ System Application, Software Version 2.0.17, Catalog Number 0694-002-090. Used for counting, displaying, recording and locating the number of RFID-tagged absorbent articles used during surgical procedures.
• Triton Canister System (finished part numbers FG 12009, for 3L canisters, and FG 12019 for 2L canisters) Scanning Label (component part number 11032). A software application used to help estimation of blood loss. Used with blood bearing canisters and accessories.
• Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6