Becton Dickinson recalls BD Blood Collection Assembly with Male Luer Lock (Catalog MBC6010) due to risk of luer breaking, causing leaks or getting stuck in dialysis ports. Affected units have specific lot numbers. Patients may need re-cannulation.
The luer could break and cause the device to leak or break off and get stuck in the fistula needle port rendering the port inaccessible for dialysis. As a result, the patient would need to be re-cannulated with a new fistula needle to obtain their dialysis treatment.
Becton Dickinson is recalling blood collection assemblies with male luer locks because the luer could break, leading to leaks or getting stuck in dialysis ports. This requires patients to re-cannulate with a new needle, which can disrupt dialysis treatment.
The luer lock component can break during use, causing the device to leak or become stuck in the fistula needle port. This makes the port inaccessible for dialysis, requiring a new needle insertion and potentially delaying treatment.
Patients using hemodialysis who have the recalled blood collection assembly with male luer lock. Those with the specific lot numbers are most at risk.
Check the catalog number MBC6010 on the product. Affected units have specific lot numbers listed in the recall notice, including combinations like 18041501 and (17)210315(10)18041501.
Look for the lot numbers listed in the recall notice, such as 18041501 or (17)210315(10)18041501.
Reach out to Becton Dickinson for guidance on next steps if you have the recalled product.
The luer lock could break, causing leaks or getting stuck in the dialysis port, which requires re-cannulation with a new needle.
Affected units have specific lot numbers including 18041501, (17)210315(10)18041501, and similar combinations listed in the recall notice.
No, but you should check the lot number and contact Becton Dickinson if you have the recalled product.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-1122-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-1122-2019 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.
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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.
