Facility

Battle Creek Equipment

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

Key facts

1recalls · worst Class II

3inspections · worst OAI

—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)	1833125
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	702 S Reed Rd Fremont, IN, US 46737
Registration status	Active · expires 2026
Parent company	Battle Creek Equipment (owner-operator 1832415)
Brand names	Good2Go; Stay-Put; Ice It!

Activity by year

Recalls (1)
Inspections (3)

Devices registered here (1)

Pack, Hot Or Cold, Reusable
Product code IME (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.5700

Recalls & enforcement

Class IITerminated2016-09-15
Products manufactured with the SPT cord have a known failure mode of sparking,causing smoke, fire and burns.

FDA inspections (3)

NAI2018-10-11
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
OAI2017-05-31
Official Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
OAI2016-02-10
Official 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.

All facilities operated by Battle Creek Equipment

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. “Battle Creek Equipment (FEI 1833125) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1833125-battle-creek-equipment/

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