Recall notification -BD Blood Collection Assembly with Male Luer Lock

Mar 7, 2019


BD is conducting a voluntary medical device recall for multiple lots of the BD Blood Collection Assembly with Male Luer Lock based on confirmed complaints of a breakage in the luer. This issue could 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.

If you require further assistance, please contact Regional Customer Quality at 888-237-2762 Opt 3, Opt 2 Monday - Friday between 8AM and 5PM (CT).

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