Facility

VITALGO 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)	3010034871
Establishment type	Complaint File Establishment per 21 CFR 820.198
Location	3315 Commerce Pkwy Miramar, FL, US 33025
Registration status	Active · expires 2026
Parent company	Vitalgo Inc. (owner-operator 10042652)
Brand names	Total Lift Bariatric Bed

Activity by year

Recalls (1)
Inspections (3)

Devices registered here (1)

Bariatric Bed
Product code OSI (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5100

Recalls & enforcement

Class IITerminated2018-04-12
Potential for unintentional movement of the support surface of the bed from tilted position to horizontal position or any position in between.

FDA inspections (3)

NAI2024-12-13
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
NAI2022-10-27
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
VAI2017-02-17
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: 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 Vitalgo 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. “VITALGO INC. (FEI 3010034871) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3010034871-vitalgo-inc/

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