# FDA recall Z-0275-2020

> **Life Technologies Corporation** · Class II · device recall initiated 2019-06-11.

## Product

CTSTM Essential 8 Medium

## Reason for recall

Component was not tested by the supplier for adventitious agents

## Distribution

StemPro¿ MSC SFM CTSTM distributed to the following states in the USA: AL, CA, CO, CT, DC, FL, GA, IA, IL, KS, MA, MD, MN, NC, NE, NJ, NY,OH, OR, PA, RI, TX, UT, VA, WA, WI.    StemPro¿ MSC SFM CTSTM distributed Internationally to the following countries: Australia, Belgium, Brazil,  Canada, Chile, China, Croatia, Czech Republic, Denmark, France, Germany, Hong Kong, India, Indonesia, Iraq, Israel, Italy, Japan, Jordan, Kazakhstan, Malaysia,  Netherlands, Pakistan, Poland, Republic of Korea, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Taiwan, Thailand, Ukraine, United Kingdom, Vietnam.    CTSTM Essential 8 Medium  distributed to the following states in the USA: CA, DC, FL, IA, IL, MA, MD, MN, NC, NY, WA, WI.    CTSTM Essential 8 Medium distributed Internationally to the following countries:  Australia, Canada, China, France, Germany, India, Japan, Netherlands, Portugal, Republic of Korea, Saudi Arabia,  Singapore, Sweden, Switzerland, Taiwan, United Kingdom.

## Key facts

- **Recall number:** Z-0275-2020
- **Recalling firm:** Life Technologies Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-11
- **Report date:** 2019-11-13
- **Termination date:** 2020-06-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Grand Island, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0275-2020

## Citation

> AI Analytics. FDA recall Z-0275-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0275-2020. Source: US FDA. Licensed CC0.

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