FDA Device recall Z-0274-2020
StemPro¿ MSC SFM CTS"
- FDA Device
- Class II
- terminated
- Published 2019-11-13
On 2019-11-13 the FDA classified a Class II recall of StemPro¿ MSC SFM CTS" 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-0274-2020 |
| 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
StemPro¿ MSC SFM CTS"
Reason
Component was not tested by the supplier for adventitious agents
Identifiers
| code_info | SKU#: A1033301; Lot # 556094 (Exp 2/28/2010), 577934 (Exp 4/30/2010) , 883643 (Exp 12/30/2011), 987595 (Exp 6/30/201…SKU#: A1033301; Lot # 556094 (Exp 2/28/2010), 577934 (Exp 4/30/2010) , 883643 (Exp 12/30/2011), 987595 (Exp 6/30/2013), 1607880 (Exp 6/30/2016), 1936294 (Exp 11/30/2019), 1960237 (Exp 4/30/2020), 2015107 (Exp 10/30/2020), 2049317 (Exp 11/30/2020), 2074105 ( Exp2/28/2021) |
|---|
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-0274-2020%22
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