Stryker recalls 50-pack of Medivac Guardian 3L blood loss inserts and scanning labels (catalog FG 12022) 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 3L 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 scanning labels may produce incorrect blood loss estimates. This could cause healthcare providers to miss or delay treatment for postpartum hemorrhage, a life-threatening condition after childbirth.
Healthcare providers using the Medivac Guardian 3L blood loss monitoring system are likely affected. Those managing obstetric care during childbirth face the highest risk due to potential delays in recognizing postpartum hemorrhage.
Check for the catalog number FG 12022 on the box. The lot numbers M2112001, M2112003, M2202001, M2203001, M2204001, M2205001, and M2206002 are also associated with this recall.
Identify the catalog number (FG 12022) and lot numbers (M2112001, M2112003, M2202001, M2203001, M2204001, M2205001, M2206002) on the box.
Stryker is recalling 50 inserts and scanning labels for the Medivac Guardian 3L blood loss monitoring system (catalog number FG 12022) that may cause inaccurate blood loss estimates.
Look for the catalog number FG 12022 and lot numbers M2112001, M2112003, M2202001, M2203001, M2204001, M2205001, or M2206002 on the box.
The recall record does not specify a remedy, so contact Stryker directly for guidance.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1185-2023 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1185-2023 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.
