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TRITON
STRYKER CORPORATION · Model GAUS-2 · UDI-DI 00859506006029
PBZ
Prescription
6
510(k) clearances
268
Adverse events
4
Recalls
2
Facilities
Description
TRITON CANISTER
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-01-25 | Stryker Corporation | Triton Canister Software, Insert & Scanning Label may cause the Triton Canister System to output inaccurate blood loss estimates can lead to confusion and could potentially result |
| 2023-01-25 | Stryker Corporation | Triton Canister Software, Insert & Scanning Label may cause the Triton Canister System to output inaccurate blood loss estimates can lead to confusion and could potentially result |
| 2023-01-25 | Stryker Corporation | Triton Canister Software, Insert & Scanning Label may cause the Triton Canister System to output inaccurate blood loss estimates can lead to confusion and could potentially result |
| 2020-01-22 | Stryker Instruments Div. of Stryker Corporation | Some Canister Scanning Labels used to calibrate the Triton Canister System have a color variance. Based on a comprehensive analysis, blood loss estimates obtained using these Canis |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.