Becton Dickinson & Company recalls BD Blood Collection Assembly with Male Luer Lock, Catalog Nu
Recalled Product
BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010
Hazard / Issue
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.
Issued by
FDA
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