Becton Dickinson recalls 8G x 10cm bone marrow needles with potential sterility issues. Product pouches may not seal properly, risking contamination during medical procedures.
Product Pouches may not be sealed properly and compromise the sterility of the device
Becton Dickinson is recalling 8G x 10cm bone marrow biopsy needles that may have pouches not sealing properly. This could lead to contamination during medical procedures if the device is used without proper sterility.
The product pouches may not seal properly, which could compromise the sterility of the device. If the device is used without proper sterility, it might lead to contamination during medical procedures.
Healthcare professionals using these needles for bone marrow procedures are most at risk. Patients receiving these needles would be affected if the sterility is compromised.
Look for the product with catalog number TMJ4008, lot number 0001159474, and expiration date August 31, 2022. The UDI code starts with (01)10885403044564.
Verify the catalog number TMJ4008, lot number 0001159474, and expiration date August 31, 2022.
The product pouches may not seal properly, which could compromise the sterility of the device during medical procedures.
The recall record does not specify a remedy, so no action is required beyond checking product details.
The recall indicates a potential sterility issue, but no specific injury mechanism is described.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2411-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2411-2019 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.