Becton Dickinson & Company recalls BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System i
Recalled Product
BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536
Hazard / Issue
Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.
Issued by
FDA
Affected States: VA
Lot/Code Info: Lot Number: 8337721 Exp. 30-Nov-2021 UDI: 382903835362
View official government recall
Were you affected by this recall?
If you were harmed by a recalled product, you may have legal options. Consider speaking with a consumer protection lawyer in your state.
Looking for safe alternatives?
Browse certified-safe products in this category on Amazon →
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime