FDAClass IIJanuary 29, 2014

AMS-530 7 Microbore Trifurcated Extension sets Product recall

AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set.

Why was AMS-530 7 Microbore Trifurcated Extension sets Product recalled?

Defective component may cause extension sets to leak.

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: 1306034, 1307011

Product
AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set.
Recalling firm
Churchill Medical Systems, Inc.
Quantity
3850
Distribution
US Nationwide Distribution in the states of: NY, VA, IL, MO, OR, FL, DE, OH
Recall date
January 29, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls