RegWardenFDA facility compliance records
Company

UTAH MEDICAL PRODUCTS, INC.

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

Recalls by year

FDA actions on record by year2013: 1 recalls; 2015: 1 recalls1’13’141’15’16’17’18’19’20’21’22’23’24’25’26
  • Recalls (2)

Registered facilities (2)

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. We restate the public record only — measured facts, never risk verdicts.

Cite this record

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

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