Reported Apr 17, 2019 · Terminated
BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010
Becton Dickinson & Company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Becton Dickinson & Company · 1 Becton Dr · Franklin Lakes, NJ · 07417-1815
Is this the product you have?
- BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010
- Lot codes and dates
- 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
- Amount recalled
- 6,509,600
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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