NAVAJO MANUFACTURING COMPANY
1 recall(s) on record — most severe on record: Class I.
Activity by year
- Recalls (1)
- Inspections (1)
Devices registered here (1)
- Tampon, Menstrual, UnscentedProduct code HEB (opens in a new tab) · Class II · Obstetrics/Gynecology · 21 CFR 884.5470
Recalls & enforcement
- Class IOngoing2026-02-18If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad under the body, then the high limit device is unable to sense the higher temperature so power is not terminated. May cause…
FDA inspections (1)
- NAI2018-07-18No Action Indicated · Compliance: Devices; Postmarket Assurance: 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. “NAVAJO MANUFACTURING COMPANY (FEI 3006140792) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006140792-navajo-manufacturing-company/
Alerts for NAVAJO MANUFACTURING COMPANY
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.