Facility

FORBES REHAB SERVICES INC.

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

Key facts

1recalls · worst Class II

3inspections · 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)	1000136418
Establishment type	Manufacture Medical Device
Location	181 Illinois Ave. South Mansfield, OH, US 44905
Registration status	Active · expires 2026
Parent company	FORBES REHAB SERVICES INC. (owner-operator 9006226)
Brand names	Forbes Rehab Services, Inc

Activity by year

Recalls (1)
Inspections (3)

Devices registered here (1)

System, Communication, Powered
Product code ILQ (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.3710

Recalls & enforcement

Class IIOngoing2021-10-11
Warning Added: Using damaged cables or chargers, or charging when moisture is present, can cause fire, electric shock, injury, or damage to Speech Generating Device or other property

FDA inspections (3)

NAI2024-12-20
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
NAI2021-10-27
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
VAI2018-07-19
Voluntary Action Indicated · Compliance: 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 FORBES REHAB SERVICES INC.

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. “FORBES REHAB SERVICES INC. (FEI 1000136418) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000136418-forbes-rehab-services-inc/

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