Facility

Heritage Medical Products, inc

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

Key facts

1recalls · worst Class II

2inspections · 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)	3003881889
Establishment type	Manufacture Medical Device
Location	10380 CR 6310 West Plains, MO, US 65775
Registration status	Active · expires 2026
Parent company	HERITAGE MEDICAL PRODUCTS, INC. (owner-operator 9057469)
Brand names	Sonobed

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (1)

Table, Examination, Medical, Powered
Product code LGX (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4960

Recalls & enforcement

Class IITerminated2016-09-02
Potential for bed to drop suddenly at the head while a patient is laying on it.

FDA inspections (2)

NAI2023-05-02
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
NAI2017-05-24
No 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 HERITAGE MEDICAL PRODUCTS, 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. “Heritage Medical Products, inc (FEI 3003881889) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003881889-heritage-medical-products-inc/

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