FDAClass IIJanuary 16, 2013

AutoPulse Resuscitation System recall

AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoPulse Model 100 Automatic Mechanical Chest compressor is…

Why was AutoPulse Resuscitation System recalled?

Complaints associated with an unexpected stop in AutoPulse compressions.

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?

all

Product
AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoPulse Model 100 Automatic Mechanical Chest compressor is…
Recalling firm
Zoll Circulation, Inc.
Quantity
3881 in US, 1846 ROW.
Distribution
Worldwide distribution.
Recall date
January 16, 2013
Classification
Class II
Status
Terminated
Agency
FDA (device)
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