Becton Dickinson & Company: Medical Device Recall in 2019 - (Recall #: Z-1122-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010

Product Classification:

Class II

Date Initiated: March 7, 2019

Date Posted: April 17, 2019

Recall Number: Z-1122-2019

Event ID: 82317

Reason for Recall:

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.

Status: Terminated

Product Quantity: 6,509,600

Code Information:

Lot Numbers, UDI: 18041501, (17)210315(10)18041501, (01)50885403235915. 18042501, (17)210325(10)18042501, (01)50885403235915. 18050501, (17)210405(10)18050501, (01)50885403235915. 18051501, (17)210415(10)18051501, (01)50885403235915. 18052501, (17)210425(10)18052501, (01)50885403235915. 18060501, (17)210505(10)18060501, (01)50885403235915. 18061501, (17)210515(10)18061501, (01)50885403235915. 18062501, (17)210525(10)18062501, (01)50885403235915. 18070501, (17)210605(10)18070501, (01)50885403235915. 18072501, (17)210625(10)18072501, (01)50885403235915. 18080501, (17)210705(10)18080501, (01)50885403235915. 18081501, (17)210715(10)18081501, (01)50885403235915.

Distribution Pattern:

US distribution to the states of FL and NJ.

Voluntary or Mandated:

Voluntary: Firm initiated