Combat Medical Systems recalls Low Titer Type O FWB Transfusion Sets with potential bent or disconnected needles. Affected units include specific lot numbers from MFG2267 to MFG3640. Stop using immediately if you own this blood kit.
There is the potential of a bent or disconnected needle in one of the components of the convenience kits.
Combat Medical Systems is recalling Low Titer Type O FWB Transfusion Sets that may have bent or disconnected needles. This could cause injury during blood administration if the kit is used without proper checks.
The transfusion set may have a bent or disconnected needle, which could cause injury during blood administration. This risk exists if the kit is used without checking the needle connection properly.
People who own or use the recalled blood transfusion kits for medical purposes are affected. Healthcare workers and patients receiving blood transfusions are most at risk.
Check for lot numbers MFG2267 through MFG3640 on the packaging. The product is a blood convenience kit for administering collected blood to patients.
Inspect the needle for bends or disconnections before use. If found, stop using the kit immediately.
Lot numbers MFG2267, MFG2347, MFG2375, MFG2430, MFG2538, MFG2637, MFG2655, MFG2693, MFG2708, MFG2754, MFG2828, MFG3120, MFG3186, MFG3340, MFG3378, MFG3386, MFG3586, MFG3640.
The recall does not provide a fix; the remedy is null. Users should check the needle connection before use.
Look for lot numbers MFG2267 through MFG3640 on the packaging. The product is a blood convenience kit for administering collected blood to patients.
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-1112-2021 — Combat Medical Systems Combat Medical Systems Hello, I own a Combat Medical Systems that is covered by recall Z-1112-2021 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.
