Becton Dickinson & Company recalls BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog N…
- Recall date
- March 1, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1710-2019
- FDA classification
- Class II
- Brand / firm
- Becton Dickinson & Company
- Sold / distributed
- US distribution to one distributor in VA.
Why it was recalled
Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536
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