MHC Medical Products, LLC
FDA adverse event reports naming MHC Medical Products, LLC as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MHC MEDICAL PRODUCTS, LLC.
- Total reports
- 2,352
- Deaths
- 0
- Injuries
- 12
- Malfunctions
- 2,340
Reports per year
Source: FDA adverse event reports by year received, 2013–2023. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Test, Blood Glucose, Over The CounterNBW1,474
- System, Measurement, Blood-Pressure, Non-InvasiveDXN405
- Syringe, PistonFMF226
- Needle, Hypodermic, Single LumenFMI183
- Single Use Only Blood Lancet With An Integral Sharps Injury Prevention FeatureFMK49
- Single (Specified) Analyte Controls (Assayed And Unassayed)JJX12
- Glucose Oxidase, GlucoseCGA3
Recent recalls
- Open, ClassifiedLabeling mix-ups
EasyTouch (ET) Insulin Syringe 29G 1ml " (Item 829155) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
The retail shelf cartons may be labeled with an incorrect lot number.
- Open, ClassifiedLabeling mix-ups
EasyTouch (ET) Insulin Syringe 29G 0.5ml " (Item 829555) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
The retail shelf cartons may be labeled with an incorrect lot number.
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