FDAClass IIFebruary 5, 2014

Compressor Mini To provide a supply of dry recall

Compressor Mini To provide a supply of dry, filtered compressed air for a medical respiratory ventilator or anaesthesia machine that meet the…

Why was Compressor Mini To provide a supply of dry recalled?

Maquet Compressor Mini may deliver compressed air at a temperature higher than specified.

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 6481779

Product
Compressor Mini To provide a supply of dry, filtered compressed air for a medical respiratory ventilator or anaesthesia machine that meet the…
Recalling firm
Maquet Cardiovascular Us Sales, Llc
Quantity
237 units
Distribution
Worldwide Distribution US, Canada and Japan.
Recall date
February 5, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
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