FDA Device recall Z-1940-2014
Stirling Ultracold Portable Shuttle, ULT-25
- FDA Device
- Class II
- terminated
- Published 2014-07-09
On 2014-07-09 the FDA classified a Class II recall of Stirling Ultracold Portable Shuttle, ULT-25 by Global Cooling, citing the external power supply input is overheating at the connection to the freezer.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1940-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-03-20 |
| Published | 2014-07-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Global Cooling |
| Distribution | AK, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, LA, MA, MD, MI, MN, MO, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA |
Product
Stirling Ultracold Portable Shuttle, ULT-25. Storage for cold-chain management, short-term or long-term ultra-low and storage and transport of biological specimens.
Reason
The external power supply input is overheating at the connection to the freezer.
Identifiers
| code_info | Codes: ULT-25-255 & ULT-25-713 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1940-2014%22
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