RegWardenFDA facility compliance records
Facility

UTAH MEDICAL PRODUCTS, LTD.

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

Activity 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)

Devices registered here (1)

  • Catheter, Peritoneal Dialysis, Single Use
    Product code FKO (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.5630

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.

Related

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, LTD. (FEI 3003105967) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003105967-utah-medical-products-ltd/

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