Stryker recalls Triton Canister Software (GAUS-2) that may cause inaccurate blood loss estimates, potentially leading to delayed recognition or prolonged postpartum hemorrhage.
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.
Stryker is recalling Triton Canister Software version 2.8.4 because it may give inaccurate blood loss estimates during childbirth. This could lead to delayed or prolonged postpartum hemorrhage, requiring more aggressive treatment.
The software may output incorrect blood loss measurements, which could cause healthcare providers to miss or delay treatment for postpartum hemorrhage. This might lead to more severe bleeding complications if not addressed promptly.
Healthcare providers using the software for blood loss estimation during childbirth are most at risk. The recall affects hospitals and clinics that use this specific software version.
Check for software version 2.8.4 labeled as 'Triton Canister Software Catalog Number: GAUS-2'. The software is used in medical settings for blood loss estimation during childbirth.
Verify the software version is 2.8.4 with catalog number GAUS-2.
The software may cause inaccurate blood loss estimates, which could lead to delayed recognition or prolonged postpartum hemorrhage, but it is not immediately dangerous.
The recall does not specify a remedy, so check the software version and contact Stryker if you need further assistance.
Inaccurate blood loss estimates could lead to delayed or prolonged postpartum hemorrhage, requiring more aggressive treatment.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1186-2023 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1186-2023 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
