FDAClass IIOctober 16, 2019

Triple Lumen Bundle KIT Ecvc1540 recall

TRIPLE LUMEN BUNDLE KIT ECVC1540

Why was Triple Lumen Bundle KIT Ecvc1540 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?

2017102650 2018010550 2018020850 2018042650 2018071650 2018081050 2018090450 2018100950 2018101750 2019032250

Product
TRIPLE LUMEN BUNDLE KIT ECVC1540
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