FDA Device recall Z-0275-2020
CTSTM Essential 8 Medium
- FDA Device
- Class II
- terminated
- Published 2019-11-13
On 2019-11-13 the FDA classified a Class II recall of CTSTM Essential 8 Medium by Life Technologies, citing component was not tested by the supplier for adventitious agents.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0275-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-11 |
| Published | 2019-11-13 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Life Technologies |
| Distribution | 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 |
Product
CTSTM Essential 8 Medium
Reason
Component was not tested by the supplier for adventitious agents
Identifiers
| code_info | SKU: A2656001 Lot: 1955886 (Exp1/30/2019), 1960951 (Exp1/30/2019), 2039735 (Exp1/30/2020) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0275-2020%22
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