Facility

HAMILTON CO.

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)	2915796
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	4970 ENERGY WAY Reno, NV, US 89502
Registration status	Active · expires 2026
Parent company	HAMILTON CO. (owner-operator 2915796)
Brand names	VERSANT Molecular System SP Module Stand Alone Sample Prep (SASP)

Activity by year

Recalls (1)

Devices registered here (1)

Clinical Sample Concentrator
Product code JJH (opens in a new tab) · Class I · Clinical Chemistry · 21 CFR 862.2310

Recalls & enforcement

Class IIOngoing2021-01-15
There is a risk that the device can start a fire if flammable liquids contact and enter the device.

All facilities operated by HAMILTON 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. “HAMILTON CO. (FEI 2915796) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2915796-hamilton-co/

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