Combat Medical Systems recalls Valkyrie LTOWB Administration blood kits with potential bent or disconnected needles. Affected kits may cause injury during blood administration. Stop using immediately if you own the recalled model.
There is the potential of a bent or disconnected needle in one of the components of the convenience kits.
Combat Medical Systems recalls blood administration kits that may have bent or disconnected needles, which could cause injury during blood transfusion. This risk affects users who have the specific lot numbers listed in the recall.
The kits may have bent or disconnected needles, which could cause injury during blood administration. This risk occurs when the needle is not properly connected or functions correctly, potentially leading to blood leakage or injury.
People who use blood administration kits for medical purposes, especially those with the specific lot numbers listed in the recall. Healthcare workers and patients receiving blood transfusions are most at risk.
Check the lot numbers on the kit: MFG3205, MFG3353, MFG3403, MFG3440, MFG3540, MFG3574, MFG3584, MFG3649, MFG3660, or MFG3698. The product is a blood convenience kit for administering blood to patients.
Look for the lot numbers MFG3205, MFG3353, MFG3403, MFG3440, MFG3540, MFG3574, MFG3584, MFG3649, MFG3660, or MFG3698 on the kit.
The kits may have bent or disconnected needles, which could cause injury during blood administration.
Check the lot numbers on the kit: MFG3205, MFG3353, MFG3403, MFG3440, MFG3540, MFG3574, MFG3584, MFG3649, MFG3660, or MFG3698.
The recall does not specify a remedy, so contact Combat Medical Systems for further instructions.
We’ve drafted a message you can send Combat Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1111-2021 — Combat Medical Systems Combat Medical Systems Hello, I own a Combat Medical Systems that is covered by recall Z-1111-2021 from Combat Medical Systems. 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.
