Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Blood Collection Assembly with Male Luer Lock Recalled by Becton Dickinson & Company Due to The luer could break and cause the device...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Becton Dickinson & Company directly.
Affected Products
BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010
Quantity: 6,509,600
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 2 states: FL, NJ
About Becton Dickinson & Company
Becton Dickinson & Company has 169 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report