Becton Dickinson recalls BD Vacutainer Push Button Blood Collection Sets with catalog number 367344 due to potential failure to meet sterility standards. Consumers should check their product details and contact the company for guidance.
Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
Becton Dickinson is recalling certain BD Vacutainer Push Button Blood Collection Sets because they may not meet the required sterility standards. This could lead to contamination of blood samples during collection, which is a serious risk for medical procedures.
The blood collection sets may not maintain sterility as claimed, potentially leading to contamination of blood samples. This could cause infections or inaccurate test results if the sets are used in medical procedures.
Healthcare professionals and individuals using these blood collection sets for medical purposes are affected. Those with medical conditions requiring frequent blood draws are at higher risk.
Check for the catalog number 367344 on the product label. The sets are sold under specific model numbers including 7346627, 7348974, 7348975, and others listed in the recall notice.
Look for the catalog number 367344 on the product label to confirm if it is recalled.
The product does not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6, which could lead to contamination of blood samples.
Check the product label for the catalog number 367344. If it matches, contact Becton Dickinson for further instructions.
The recall is due to potential contamination of blood samples, not a physical injury risk. However, improper use could lead to inaccurate test results or infections.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-1532-2018 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-1532-2018 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.
