Stryker recalls 50-pack of Medivac Guardian 2L blood loss inserts and labels (catalog FG 12010) that may cause inaccurate blood loss estimates, risking delayed treatment of 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 50 inserts and scanning labels for the Medivac Guardian 2L blood loss monitoring system. These items may cause inaccurate blood loss measurements, which could delay or worsen postpartum hemorrhage treatment.
The software in the inserts and labels may produce incorrect blood loss estimates. This could lead to delayed recognition or prolonged postpartum hemorrhage, requiring more aggressive medical intervention.
Healthcare providers using the Medivac Guardian 2L blood loss monitoring system with the recalled inserts and labels are most at risk. This affects hospitals and clinics that use the system during childbirth.
Check for the catalog number FG 12010 on the box. The lot numbers M2110004, M2201002, M2202001, M2203002, and M2206001 are affected. These items were sold with the Medivac Guardian 2L system.
Verify the catalog number (FG 12010) and lot numbers (M2110004, M2201002, M2202001, M2203002, M2206001) to confirm if your items are recalled.
Stryker is recalling 50 inserts and scanning labels for the Medivac Guardian 2L blood loss monitoring system (catalog number FG 12010) that may cause inaccurate blood loss estimates.
The recalled items may cause inaccurate blood loss measurements, which could delay recognition or worsen postpartum hemorrhage, requiring more aggressive treatment.
Check for catalog number FG 12010 and lot numbers M2110004, M2201002, M2202001, M2203002, or M2206001 on the box.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1184-2023 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1184-2023 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.
