Facility

SECHRIST INDUSTRIES, INC.

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

Key facts

2recalls · 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)	2020676
Establishment type	Manufacture Medical Device
Location	4225 E LA PALMA AVE Anaheim, CA, US 92807
Registration status	Active · expires 2026
Parent company	SECHRIST INDUSTRIES, INC. (owner-operator 2020676)
Brand names	Hyperbaric Electronic Records Organizer (H.E.R.O.); eHEAL

Activity by year

Recalls (2)
Inspections (2)

Devices registered here (1)

Medical Device Data System
Product code OUG (opens in a new tab) · Class I · General Hospital · 21 CFR 880.6310

Recalls & enforcement

Class IITerminated2015-06-01
Sechrist Industries is recalling the Sechrist Low Profile Wheeled Stretcher because it may experience an unexpected incline angle during the height adjustment of the Low Profile Wheeled Stretcher when lifting the patient upward or when lowering the Wheeled Stretcher to a height a…
Class IITerminated2008-08-28
Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of the chamber.

FDA inspections (2)

NAI2022-09-14
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
VAI2017-12-15
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 SECHRIST INDUSTRIES, 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. “SECHRIST INDUSTRIES, INC. (FEI 2020676) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2020676-sechrist-industries-inc/

Not open yet

Alerts for SECHRIST INDUSTRIES, INC.

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.