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).


Files available for download

This site uses cookies. If you click accept cookies then all cookies will be written. Please review our cookies policy and configure your cookies for your experience.