Facility

CARDINAL SCALE MFG. CO.

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

Key facts

1recalls · worst Class II

1inspections · worst VAI

—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)	1929045
Establishment type	Manufacture Medical Device
Location	102 EAST DAUGHERTY Webb City, MO, US 64870
Registration status	Active · expires 2026
Parent company	CARDINAL SCALE MFG. CO. (owner-operator 1929045)
Brand names	Detecto

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Scale, Platform, Wheelchair
Product code INF (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3940

Recalls & enforcement

Class IITerminated2015-12-23
One complaint of a seat on a scale failing unexpectedly which can cause an injury.

FDA inspections (1)

NAI2017-03-31
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 CARDINAL SCALE MFG. CO.

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. “CARDINAL SCALE MFG. CO. (FEI 1929045) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1929045-cardinal-scale-mfg-co/

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