Facility

Navajo Manufacturing Company Inc.

1 recall(s) on record — most severe on record: Class I.

Key facts

1recalls · worst Class I

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	1000065475
Establishment type	Complaint File Establishment per 21 CFR 820.198
Location	5330 FOX ST. Denver, CO, US 80216
Registration status	Active · expires 2026
Parent company	Navajo Manufacturing Company Inc. (owner-operator 1720839)
Brand names	Ice Bag

Activity by year

Recalls (1)

Devices registered here (1)

Bag, Ice
Product code KYR (opens in a new tab) · Class I · General Hospital · 21 CFR 880.6050

Recalls & enforcement

Class IOngoing2026-02-18
If 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…

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 Inc. (FEI 1000065475) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000065475-navajo-manufacturing-company-inc/

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