Reported Jun 12, 2019 · Terminated
BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog…
Becton Dickinson & Company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Becton Dickinson & Company · 1 Becton Dr · Franklin Lakes, NJ · 07417-1815
Is this the product you have?
- BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral
- vascular system Catalog Number383536
- Lot codes and dates
- Lot Number8337721 Exp. 30-Nov-2021
- UDI382903835362
- Amount recalled
- 6,720 units
Where it was sold
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.
This product could cause temporary or reversible health problems — stop using it.
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