FDAClass IIOctober 16, 2019

OR Vantex 7fr 3l 16cm CVC Ecvc6665 recall

OR VANTEX 7FR 3L 16CM CVC ECVC6665

Why was OR Vantex 7fr 3l 16cm CVC Ecvc6665 recalled?

Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.

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?

2018111950 2019031350 2019040550

Product
OR VANTEX 7FR 3L 16CM CVC ECVC6665
Recalling firm
Centurion Medical Products Corporation
Quantity
181965 total
Distribution
Nationwide domestic distribution.
Recall date
October 16, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls