BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter recall
BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536
Why was BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Number: 8337721 Exp. 30-Nov-2021 UDI: 382903835362
- Product
- BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536
- Recalling firm
- Becton Dickinson & Company
- Quantity
- 6,720 units
- Distribution
- US distribution to one distributor in VA.
- Recall date
- June 12, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)