C.A. Greiner recalls VACUETTE Blood Transfer Units with lot A19024NX (expired Feb 2022) due to needle dislodgement causing potential needle stick injuries or blood leakage during blood transfer.
While transferring blood the needle may dislodged and remain in the tube stopper which may cause needle stick injury or blood leakage.
C.A. Greiner is recalling VACUETTE Blood Transfer Units with lot number A19024NX that expired February 2022. The units may cause needle stick injuries or blood leakage if the needle dislodges from the tube stopper during blood transfer.
During blood transfer from a syringe to the collection tube, the needle may become dislodged and remain in the tube stopper. This can cause needle stick injuries or blood leakage, potentially leading to infection or injury.
People who own or use the VACUETTE Blood Transfer Unit with lot number A19024NX (expired February 2022) are affected. Healthcare professionals and patients using this unit for blood collection are most at risk.
Check for the lot number A19024NX on the unit. The product expired February 2022 and was sold with item number 450225.
Look for the lot number A19024NX on the VACUETTE Blood Transfer Unit.
Contact C.A. Greiner directly for further instructions on handling the recalled unit.
The recall indicates a potential risk of needle stick injuries or blood leakage during use, so it should not be used until the manufacturer provides instructions.
Check for the lot number A19024NX and contact C.A. Greiner for further instructions.
The recalled unit has lot number A19024NX and expired February 2022.
We’ve drafted a message you can send C.A. Greiner to request your refund or repair — edit it as you like.
Subject: Recall Z-2116-2020 — C.A. Greiner C.A. Greiner Hello, I own a C.A. Greiner that is covered by recall Z-2116-2020 from C.A. Greiner. 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.
