Medi-Therm Hyper/Hypothermia System, MTA7900
Reported: May 17, 2017 Initiated: March 29, 2017 #Z-2058-2017
Product Description
Medi-Therm Hyper/Hypothermia System, MTA7900
Reason for Recall
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.
Details
- Recalling Firm
- Stryker Medical Division of Stryker Corporation
- Units Affected
- 119
- Distribution
- USA (nationwide) Distribution and Internationally to Colombia.
- Location
- Portage, MI
Frequently Asked Questions
What product was recalled? ▼
Medi-Therm Hyper/Hypothermia System, MTA7900. Recalled by Stryker Medical Division of Stryker Corporation. Units affected: 119.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 17, 2017. Severity: Moderate. Recall number: Z-2058-2017.
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