MHC Medical Products
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (3)
Devices registered here (1)
- Needle, Hypodermic, Single LumenProduct code FMI (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5570
Recalls & enforcement
- Class IIOngoing2018-04-06The retail shelf cartons may be labeled with an incorrect lot number.
FDA inspections (3)
- NAI2025-02-26No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
- NAI2022-09-23No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- VAI2018-02-02Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “MHC Medical Products (FEI 3005798905) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3005798905-mhc-medical-products/
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