Diagnostica Stago recalls STA Noplastine CI Plus 10ml vials for potential prolonged prothrombin time due to QC values outside assigned ranges. Affected lots include 250791-252737 with specific expiration dates.
QC values outside of the assigned ranges (prolonged Prothrombin time / decreased PT %)
Diagnostica Stago is recalling its STA Noplastine CI Plus 10ml vials for in-vitro diagnostic use. The recall is due to QC values outside the assigned ranges, which could cause prolonged prothrombin time. This may lead to inaccurate blood clotting tests if used without proper calibration.
The vials may produce QC values outside the assigned ranges, leading to prolonged prothrombin time. This could result in inaccurate blood clotting test results if used without proper calibration.
Users of this blood clotting test kit for in-vitro diagnostics are affected. Healthcare professionals and labs using the STA Noplastine CI Plus vials for prothrombin time testing are most at risk.
Check for vial lot numbers 250791 through 252737 with expiration dates from July 2018 to September 2019. The product is sold as an in-vitro diagnostic for prothrombin time testing.
Look for lot numbers 250791 through 252737 on the vial label.
Diagnostica Stago STA Noplastine CI Plus 10ml vials for in-vitro diagnostic use of prothrombin time testing.
The vials may produce QC values outside the assigned ranges, potentially causing prolonged prothrombin time and inaccurate blood clotting test results.
Check the vial lot numbers 250791 through 252737 with expiration dates from July 2018 to September 2019.
We’ve drafted a message you can send Diagnostica Stago to request your refund or repair — edit it as you like.
Subject: Recall Z-2993-2018 — Diagnostica Stago Diagnostica Stago Hello, I own a Diagnostica Stago that is covered by recall Z-2993-2018 from Diagnostica Stago. 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.
