FDAClass IIISeptember 10, 2014

LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group recall

LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group

Why was LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group recalled?

During label reconciliation a duplicate serial number label was detected to be printed for the LINEAR 7.5 FR 40 cc Intra-Aortic Balloon Catheter.

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?

Part Number - 0684-00-0480-01U

Product
LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group
Recalling firm
Datascope Corporation
Quantity
one unit
Distribution
US Distribution to TX.
Recall date
September 10, 2014
Classification
Class III
Status
Terminated
Agency
FDA (device)
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