Facility

The Brewer Company LLC

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

Key facts

1recalls · worst Class II

1inspections · worst NAI

—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)	2182536
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	W165N5830 Ridgewood Dr. MENOMONEE FALLS, WI, US 53051
Registration status	Active · expires 2026
Parent company	The Brewer Company LLC (owner-operator 2182536)

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Mattress, Flotation Therapy, Non-Powered
Product code IKY (opens in a new tab) · Class I · General Hospital · 21 CFR 880.5150

Recalls & enforcement

Class IITerminated2018-03-29
One lot, the wire harness was over-crimped on some of the connectors that go to the two vertical side switches on the exam table.

FDA inspections (1)

NAI2025-05-22
No 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.

All facilities operated by The Brewer Company LLC

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. “The Brewer Company LLC (FEI 2182536) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2182536-the-brewer-company-llc/

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