Greiner Bio-One recalls VACUETTE blood collection tubes that may show insufficient draw volume, leading to inaccurate coagulation test results. Affected tubes have specific model numbers and expiration dates.
VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% may show insufficient draw volume of the tubes, which could produce erroneous results for prothrombin time, activated partial thromboplastin time, and fibrinogen assays.
Greiner Bio-One is recalling VACUETTE blood collection tubes that may not draw enough blood, causing inaccurate coagulation test results. This could lead to incorrect medical diagnoses if used for blood tests.
These tubes may not draw sufficient blood, which can cause test results for prothrombin time, activated partial thromboplastin time, and fibrinogen to be inaccurate. This may lead to incorrect medical diagnoses or treatment decisions.
People who use these blood collection tubes for coagulation testing, such as lab technicians or medical professionals, are most at risk of inaccurate test results.
Check for the model number 9NC Coagulation sodium citrate 3.2% with a blue cap and white ring. The tubes have specific expiration dates: February 2022 through March 2022.
Verify the expiration date on the tube label to ensure it matches the dates listed in the recall (February 2022 through March 2022).
Look for the model number 9NC Coagulation sodium citrate 3.2% with a blue cap and white ring on the tube.
The tubes may not draw enough blood, leading to inaccurate coagulation test results for prothrombin time, activated partial thromboplastin time, and fibrinogen assays.
Check the expiration date and model number to see if they are affected. If they are, you may need to use a different tube for accurate test results.
No, the tubes do not pose a physical safety risk like cuts or fires, but they can cause inaccurate test results if used improperly.
We’ve drafted a message you can send Greiner Bio-One to request your refund or repair — edit it as you like.
Subject: Recall Z-1534-2021 — Greiner Bio-One Greiner Bio-One Hello, I own a Greiner Bio-One that is covered by recall Z-1534-2021 from Greiner Bio-One. 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.
