FDAClass IIJanuary 29, 2020

Henry Schein CardioChek Starter Kit recall

Henry Schein CardioChek Starter Kit, Reference Number 4060 HS, 570-1036

Why was Henry Schein CardioChek Starter Kit recalled?

One brand of batteries have a small dimensional difference in the negative button terminal, which, when the batteries are inserted incorrectly, can create the possibility for the battery terminals to make reverse contact. This reverse contact can cause a potential for overheating.

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 Serial Numbers shipped during the 11/1/2016 to 10/25/2019 timeframe. UDI: 00304040040539

Product
Henry Schein CardioChek Starter Kit, Reference Number 4060 HS, 570-1036
Recalling firm
Polymer Technology Systems, Inc.
Quantity
44,448
Distribution
The products were distributed US Nationwide. The products were distributed to the following foreign countries: Australia, Austria, Belgium, Bermuda, Canada, China, Chile, Costa Rica, Cayman Islands, Czech Republic, England, Finland, France, Germany, Greece, Hong Kong, India, Iraq, Italy, Jordan, Lebanon, Lithuania, Mexico, Morocco, Panama, Philippines, Poland, Qatar, Romania, Saudi Arabia, South Africa, South Korea, Spain, Sweden, Switzerland, Trinidad, UAE.
Recall date
January 29, 2020
Classification
Class II
Status
Terminated
Agency
FDA (device)
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