Reported May 17, 2017 · Terminated

Medi-Therm Hyper/Hypothermia System, MTA7900

Stryker Medical Division of Stryker Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Stryker Medical Division of Stryker Corporation · 3800 E Centre Ave · Portage, MI · 49002-5826

Is this the product you have?

  • Medi-Therm Hyper/Hypothermia System, MTA7900
Lot codes and dates
  • Serial Numbers

    119 of 119 codes

    • 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
Amount recalled
119

Where it was sold

  • Nationwide

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 18, 2017 · Data as of Sep 19, 5:25 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.