Micro-Temp LT 749Recalls & reported problems
Gentherm Medical, LLC · MICRO-TEMP® LT Model 749 Localized Heat Therapy System. · Class 2
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jul 19, 2019Terminated
Updated Manual-Warnigs have been added stating that exceeding 40'C for extended periods may cause tissue damage
Z-2291-2019 · Root cause: Under Investigation by firm · FDA record ↗
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- DONJOY 11-9099Djo, LLC · Pack, hot or cold, water circulating1 recall0 reports
- DONJOY 11-1424Djo, LLC · Pack, hot or cold, water circulating1 recall0 reports
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- MEDLINE MDSCC20Medline Industries, Inc. · Pack, hot or cold, water circulating5 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.