FDAClass IIAugust 20, 2014

Prisma M 100 PRE set. Product number 103657. Each set recall

Prisma M 100 PRE set. Product number 103657. Each set is packaged in a plastic pouch, 4 pouches per carton box

Why was Prisma M 100 PRE set. Product number 103657. Each set recalled?

Gambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.

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?

Prisma M 100 PRE set. Product number 103657. Batch number 12A0302G to 14B2102. Expiry 01/2014 to 02/2016

Product
Prisma M 100 PRE set. Product number 103657. Each set is packaged in a plastic pouch, 4 pouches per carton box
Recalling firm
Gambro Renal Products, Incorporated
Quantity
401,451
Distribution
Worldwide Distribution.
Recall date
August 20, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
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