FDAJanuary 25, 2023device
Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the estimation of blood loss.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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 in either delayed recognition or prolongation of postpartum hemorrhage (PPH), or require more aggressive treatment for PPH.
What to do
FDA enforcement status: Ongoing
Brands named
stryker
UPCs
00859506006029
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDABARD Dynamic Tip Steerable, Product Number 6DYNTP001;2026-04-10
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- FDADaig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
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