Facility

SECA CORP.

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

Key facts

1recalls · worst Class II

—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)	1120986
Establishment type	Complaint File Establishment per 21 CFR 820.198
Location	13601 Benson Ave Chino, CA, US 91710
Registration status	Active · expires 2026
Parent company	SECA (owner-operator 8010918)
Brand names	seca mBCA 525; seca analytics 125

Activity by year

Recalls (1)

Devices registered here (1)

Analyzer, Body Composition, Exempt
Product code PUH (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.2770

Recalls & enforcement

Class IIOngoing2019-06-19
It has been determined that the wheels on the baby scale cart can unexpectedly loosen and in the worst case, detach from the cart completely. If this occurs the cart can become unstable and tip over, potentially leading to the scale falling from the cart. If a baby is left unatt…

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. “SECA CORP. (FEI 1120986) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1120986-seca-corp/

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