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Becton Dickinson & Company recalls BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010
Recalled April 17, 2019 · FDA recall Z-1122-2019 · Becton Dickinson &
Hazard
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. · FDA Class II
Units
6,509,600
Sold at
US distribution to the states of FL and NJ.
Description
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.
Product
BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →