Becton Dickinson recalls BD Vacutainer Push Button Blood Collection Sets that may not meet sterility claims. Products could risk contamination during blood collection.
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 might not be sterile enough for blood collection. This could lead to contamination risks if used improperly.
The product does not meet the labeled sterility claim of a Sterility Assurance Level (SAL) :10-6. This means the blood collection sets might not be sterile enough to prevent contamination during use.
Healthcare professionals and individuals using blood collection sets for medical purposes. Those most at risk are people handling the product without proper sterility checks.
Look for the product with catalog number 367342. The sets are 0.6 x 19 mm x 305 mm, 23G, and 12 units. They were sold with specific serial numbers listed in the recall notice.
Verify the catalog number and physical dimensions to confirm if your set is recalled.
The product does not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6, which could risk contamination during blood collection.
Check the catalog number and physical dimensions to confirm if your set is recalled. If it matches, contact Becton Dickinson for further instructions.
The recall is for sterility issues, not physical injury risks. There is no mention of serious injury in the recall notice.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-1531-2018 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-1531-2018 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.
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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.
