FDA Device recall Z-2970-2026
Blanketrol III, Model 233
- FDA Device
- Class II
- ongoing
- Published 2026-08-26
On 2026-08-26 the FDA classified a Class II recall of Blanketrol III, Model 233 by Gentherm Medical, citing overheating of the 115V CPU board may cause the device to shut down.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2970-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-13 |
| Published | 2026-08-26 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Gentherm Medical |
| Distribution | US |
Product
Blanketrol III, Model 233; Thermal regulating system.
Reason
Overheating of the 115V CPU board may cause the device to shut down.
Identifiers
| code_info | UDI: 1061303186102, UDI: 1061303186107, UDI: 1061303186139, UDI: 1061303187107, UDI: 1061303187307, Serial Numbers:131-2-00580 through 262-3-20277 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2970-2026%22
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