FDA Device recall Z-1186-2023
Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the estimation of blood loss
- FDA Device
- Class II
- ongoing
- Published 2023-03-08
On 2023-03-08 the FDA classified a Class II recall of Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the estimation of blood loss by Stryker, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1186-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-01-25 |
| Published | 2023-03-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Stryker |
| Distribution | US |
Product
Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the estimation of blood loss.
Reason
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.
Identifiers
| code_info | UDI-DI: 00859506006029 Software Version: 2.8.4 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1186-2023%22
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