FDAClass IIMay 31, 2017

CytoGuard Closed Luer Connector recall: Sterility Concern

CytoGuard Closed Luer Connector, Intravenous access 2 cartons of 50 units each (100 units per case)

Why was CytoGuard Closed Luer Connector recalled?

B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector due to a potential for some blisters to be punctured resulting in a compromised sterility barrier.

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 # 1240156001, 1240156002, 1240156003, 1240156004, 1370249001, 1370251101, 1370257101, 1370259201, 1370268401, 1370270401, 1370273801, 1470311101, and 1570315301

Product
CytoGuard Closed Luer Connector, Intravenous access 2 cartons of 50 units each (100 units per case)
Recalling firm
B Braun Medical Inc
Quantity
417,600 units
Distribution
United States Nationwide distribution
Recall date
May 31, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls