Facility

UTAH MEDICAL PRODUCTS, INC.

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

Key facts

2recalls · 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)	1718873
Establishment type	Manufacture Medical Device
Location	7043 South 300 West Midvale, UT, US 84047
Registration status	Active · expires 2026
Parent company	UTAH MEDICAL PRODUCTS, INC. (owner-operator 1718873)
Brand names	SOFT TOUCH

Activity by year

Recalls (2)

Devices registered here (1)

Extractor, Vacuum, Fetal
Product code HDB (opens in a new tab) · Class II · Obstetrics/Gynecology · 21 CFR 884.4340

Recalls & enforcement

Class IITerminated2015-10-16
Utah Medical is conducting a recall of Myelo-Nate CSF Sampling Kit due to an internal post-sterilization inspection that found a sterile finished tray where the seal between the Tyvek lid and the PETG tray on one side of the tray had been compromised.
Class IITerminated2013-06-04
Utah Medical Products, Inc. is recalling certain Deltran Disposable Pressure Transducer Kits due to complaints related to packaging integrity of the sterile packaged devices.

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. “UTAH MEDICAL PRODUCTS, INC. (FEI 1718873) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1718873-utah-medical-products-inc/

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