The Recall Desk

State

Utah product recalls

73,738 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total
4,914
Critical
524
Severe
1,350
Most recent
2026-10-28

Of the 4,914 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,350 (27%) are Severe.

These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31751–31775 of 78652

  • HighFDA (Food)·F-0753-2020·2020-03-04

    Lotte Choco Pie Recalled for Undeclared Almond Allergen

    Lotte Choco Pie Original is being recalled because FDA testing found undeclared almond protein in the product.

    Product
    Lotte Choco Pie Original, 12 pack 11.85 oz. (336 g) UPC: 8 801062 160709 Distributed by Lotte International America, Los Angeles, CA Product of Korea Contains: Wheat, soy, Egg. Manufactured in a facility that also processes Almond, Peanut.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1376-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i, LLC is recalling specific lots of Bellatek Encode Healing Abutments because they may produce incorrect rotation or margin contour misalignment in scanned data.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 5MM(P) X 4MM(H) Reference Number: IEHA454
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1377-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 5MM(P) X 6MM(H) Reference Number: IEHA456
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1375-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 5MM(P) X 3MM(H) Reference Number: IEHA453
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1380-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 6MM(H) Reference Number: IEHA466
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0784-2020·2020-03-04

    Lifetime Fitness D. Tox Shake Mix Recalled for Unapproved Herbicide

    Pro-Form Manufacturing LLC is recalling Lifetime Fitness D. Tox Shake Mix because the flax seed used in the product contains an unapproved herbicide.

    Product
    Lifetime Fitness D. Tox Shake Mix; Plant-Based Protein Blend. Dietary Supplement - Net Wt. 2.50 lb. (40 oz.) 1.13 kg One gallon White HDPE Jar Natural Chocolate Flavor UPC: 6 82471 00830-5 Product number: 6142-2644 Manufactured exclusively for: Life Time Fitness Inc.…
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0778-2020·2020-03-04

    Nature's Sunshine SmartMeal Shake Mix Recalled for Unapproved Herbicide in Flax Seed

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine SmartMeal Nutritional Shake Mix because the flax seed used in the product contains an unapproved herbicide.

    Product
    Nature's Sunshine SmartMeal Nutritional Shake Mix; Natural Chocolate Flavor Net Wt. 1 lb. 3.5 oz. (555 Grams) UPC: 0 99904 03084 8 Product number: 6116 US3084 Distributed exclusively by: Nature's Sunshine Products, Inc. Spanish Fork, UT 84660
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1367-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Misalignment

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.

    Product
    CERTAIN¿ BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 4MM(H) Reference Number: IEHA344
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1368-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 6MM(H) Reference Number: IEHA346
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1364-2020·2020-03-04

    Exactech Recalls Truliant Splined Stem Extensions Due to Labeling Error

    Exactech is recalling four Truliant Splined Stem Extensions because the labels incorrectly identify the implant size as 17mm x 80mm instead of 18mm x 120mm.

    Product
    Truliant Splined Stem Extension, 18mm x 120mm - Product Usage: The devices are used in a cemented total knee prosthesis system, which provides femoral components, tibial inserts, stems, augments, and surgical instrumentation for use in primary and revision total knee…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1386-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i, LLC is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour misalignment in scanned data.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 4MM(H) Reference Number: IEHA564
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1385-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i, LLC is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation and margin contour misalignment in scanned data.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 4MM(H) Reference Number: IEHA564
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1388-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 7.5MM(P) X 4MM(H) Reference Number: IEHA574
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0783-2020·2020-03-04

    Lifetime Fitness D. Tox Shake Mix Recalled for Unapproved Herbicide

    Pro-Form Manufacturing LLC is recalling Lifetime Fitness D. Tox Shake Mix because the flax seed used in the product contains an unapproved herbicide.

    Product
    Lifetime Fitness D. Tox Shake Mix; Plant-Based Protein Blend. Dietary Supplement - Net Wt. 2.36 lb. (37.76 oz.) 1.07 kg Program Kit - Natural Vanilla Flavor UPC: 6 82471 00831-2 Product number: 6142-2646 Manufactured exclusively for: Life Time Fitness Inc. 2902…
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1371-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Misalignment

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin contour misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 6MM(H) Reference Number: IEHA356
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1387-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 6MM(H) Reference Number: IEHA566
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1379-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because the resulting impression or scanned data may cause incorrect rotation and margin contour misalignment.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 4MM(H) Reference Number: IEHA464
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0779-2020·2020-03-04

    Nature's Sunshine NutriSmart Vanilla Powder Recalled for Unapproved Herbicide

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine NutriSmart Vanilla Powder because the flax seed ingredient contains an unapproved herbicide.

    Product
    Nature's Sunshine NutriSmart Polvo Para Preparar Bebida Sabor Vainilla Con In Toque Sabor a Chocolate; Vainilla Flavor Contenido Neto 510 g UPC: 0 99904 61532 8 Product number: 6116-MX61532 Importado y Distribuido por: Nature's Sunshine Products de Mexico, S.A. de C.…
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1349-2020·2020-03-04

    Randox RX Daytona Plus Clinical Chemistry Analyzer Software Recall

    Randox Laboratories is recalling RX Daytona Plus clinical chemistry analyzers to fix software issues causing incorrect sample ordering and quality control flags.

    Product
    RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Product Usage: A fully automated, random access, clinical chemistry analyzer complete with dedicated analyzer software. For use in clinical laboratories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1363-2020·2020-03-04

    Siemens ADVIA Chemistry Lipase Recalled for Calibration Failures

    Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Lipase reagents due to customer complaints about failed calibrations and increased imprecision in quality control and patient samples.

    Product
    ADVIA Chemistry Lipase, Ref. No. 01984894 B01-4840-01, Siemens Material No. 10311896, UDI 00630414482446 - Product Usage: Lipase measurements are used in the diagnosis and treatment of diseases of the pancreas, such as acute pancreatitis and obstruction of the pancreatic duct.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1382-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 5.6MM(P) X 3MM(H) Reference Number: IEHA553
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0782-2020·2020-03-04

    Nature's Sunshine SmartMeal Shake Mix Recalled for Unapproved Herbicide

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine SmartMeal Nutritional Shake Mix because the flax seed ingredient contains an unapproved herbicide.

    Product
    Nature's Sunshine SmartMeal Nutritional Shake Mix; Natural Vanilla Flavor Net Wt. 1 lb. 2 oz. (510 g) UPC: 0 99904 03085 5 Product number: 6116-US3085 Distributed by: Nature's Sunshine Products Inc. 1655 North Main Spanish Fork, UT 84660
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1345-2020·2020-03-04

    Philips DigiTrak XT Holter Recorder Software Recall for Malfunction

    Philips is recalling DigiTrak XT Holter Recorders because a software defect causes the device to fail when an AAA battery is present.

    Product
    Philips DigiTrak XT Holter Recorder Software version number B.1 and C.2. The DigiTrak XT Recorder is available in four different configurations. Service tag numbers for these configurations are as follows: - 453564067151 24-Hour Configuration - 453564067161 48-Hour…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1366-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 3MM(H) Reference Number: IEHA343
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0780-2020·2020-03-04

    Nature's Sunshine CMapt M SmartMeal Recalled for Unapproved Herbicide in Flax Seed

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine CMapt M SmartMeal products because the flax seed used contains an unapproved herbicide.

    Product
    Nature's Sunshine CMapt M - Cmapt Mi- SmartMeal; Bahu bhbhi - Vanilla; 510 g UPC: 0 99904 03085 5 Product number: 6116-RU3085 6116-UA3085 Distributed in Russia and Ukraine - same label Nature's Sunshine Products Inc. 2500 West Executive…
    Category
    Food
    Distribution
    2 states