FDA Device recall Z-2058-2017
Medi-Therm Hyper/Hypothermia System, MTA7900
- FDA Device
- Class II
- terminated
- Published 2017-05-17
On 2017-05-17 the FDA classified a Class II recall of Medi-Therm Hyper/Hypothermia System, MTA7900 by Stryker Medical Division, citing the water may reheat too quickly if the unit is in "Automatic" mode, switched to "Manual" mode to view water temperature, and then switched back to "Automatic" mode.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2058-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-29 |
| Published | 2017-05-17 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
Product
Medi-Therm Hyper/Hypothermia System, MTA7900
Reason
The water may reheat too quickly if the unit is in "Automatic" mode, switched to "Manual" mode to view water temperature, and then switched back to "Automatic" mode.
Identifiers
| code_info | Serial Numbers MTA7900A01004 MTA7900A01021 MTA7900A01029 MTA7900A01036 MTA7900A01037 MTA7900A80003 MTA7900A80004…Serial Numbers MTA7900A01004 MTA7900A01021 MTA7900A01029 MTA7900A01036 MTA7900A01037 MTA7900A80003 MTA7900A80004 MTA7900A80011 MTA7900A80016 MTA7900A80026 MTA7900A80027 MTA7900A80029 MTA7900A80030 MTA7900A80034 MTA7900A80035 MTA7900A80045 MTA7900A90006 MTA7900A90009 MTA7900A90023 MTA7900B90011 MTA7900B90019 MTA7900B90034 MTA7900B90036 MTA7900B90039 MTA7900C01016 MTA7900C01017 MTA7900D01015 MTA7900D01025 MTA7900D01029 MTA7900D80004 MTA7900D80018 MTA7900D80026 MTA7900D80030 MTA7900D80034 MTA7900D80035 MTA7900D80040 MTA7900E01018 MTA7900E01020 MTA7900E01023 MTA7900E01026 MTA7900E01028 MTA7900E01030 MTA7900E01034 MTA7900E01036 MTA7900E01041 MTA7900E80013 MTA7900E80047 MTA7900E80068 MTA7900E80077 MTA7900E90018 MTA7900E90028 MTA7900F01001 MTA7900F01007 MTA7900F01013 MTA7900F01015 MTA7900F01026 MTA7900F01035 MTA7900F01036 MTA7900F01038 MTA7900F01042 MTA7900F01049 MTA7900F01052 MTA7900F90019 MTA7900F90027 MTA7900F90030 MTA7900G0 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2058-2017%22
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