Becton Dickinson recalls 65-unit PST Gel and Lithium Heparin blood collection tubes due to false carboxyhemoglobin results when used with IL GEM 40:00 blood gas analyzers. Affected tubes have catalog number 367961.
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
Becton Dickinson is recalling 65-unit blood collection tubes that can cause false high readings of carboxyhemoglobin when tested with certain blood gas analyzers. This could lead to incorrect medical diagnoses if not addressed.
These tubes can produce false high readings of carboxyhemoglobin (COHb) when analyzed with the IL GEM 4000 blood gas instrument. This may cause incorrect medical diagnoses if the false results are not recognized.
Healthcare professionals using BD Vacutainer blood collection tubes with IL GEM 4000 analyzers may be affected. Patients receiving blood tests using these tubes could also be impacted.
Check for BD Vacutainer PST Gel and Lithium Heparin (LH) 65-unit blood collection tubes with catalog number 367961. The unique device identifier (UDI) is (01)30382903679615.
Look for catalog number 367961 on the tube packaging or label.
False elevation of carboxyhemoglobin (COHb) results have been reported when using these tubes with the IL GEM 4000 blood gas analyzer.
The recall record does not specify a remedy, so no action is required at this time.
The recall record does not mention patient risks, but incorrect results could lead to misdiagnosis.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2302-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2302-2019 from Becton Dickinson. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
