Recall notification - BD Nexiva Dual Port 18GA 1.25 IN Closed IV Catheter System

Aug 23, 2018


BD is conducting a voluntary medical device recall of the BD Nexiva Catheter lot referenced in the table above. The recall is being conducted due to reports of needle tip shield/safety mechanism issues which could result in a healthcare worker potentially being exposed to a contaminated needle stick injury after the catheter insertion process.

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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