FOLSOM METAL PRODUCTS, INC.
2 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (2)
- Inspections (4)
Devices registered here (1)
- Retainer, SurgicalProduct code GCZ (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4800
Recalls & enforcement
- Class IIOngoing2025-08-21Labeling includes shelf life that has not been validated.
- Class IIOngoing2023-10-30Units were not intended for commercial distribution and inadvertently distributed.
FDA inspections (4)
- VAI2025-08-01Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- VAI2024-08-09Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- NAI2017-11-13No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
- NAI2016-10-17No Action Indicated · Compliance: Devices
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. “FOLSOM METAL PRODUCTS, INC. (FEI 3006803588) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006803588-folsom-metal-products-inc/
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