# FDA recall Z-0835-2020

> **Polymer Technology Systems, Inc.** · Class II · device recall initiated 2019-12-02.

## Product

Henry Schein CardioChek Plus Professional Analyzer, New Analyzer, boxed, with carrying case, Reference Number 4060 HS, 570-0411

## Reason for recall

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.

## 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.

## Key facts

- **Recall number:** Z-0835-2020
- **Recalling firm:** Polymer Technology Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-02
- **Report date:** 2020-01-29
- **Termination date:** 2020-07-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Indianapolis, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0835-2020

## Citation

> AI Analytics. FDA recall Z-0835-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0835-2020. Source: US FDA. Licensed CC0.

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