FDAMarch 7, 2019device

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

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Terminated

Brands named

becton dickinsonbectonbecton dickinson

UPCs

50885403235915

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010 — Recall Details · AllClear