The Recall Desk

State

Utah product recalls

73,827 recalls have nationwide distribution and so reach Utah. 4,916 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total
4,916
Critical
524
Severe
1,351
Most recent
2026-11-04

Of the 4,916 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 1,351 (27%) are Severe.

Which agencies issued them

These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47476–47500 of 78743

  • SevereFDA (Devices)·Z-1436-2017·2017-03-15

    Siemens Medical Linear Accelerators Recalled for Defective Overhead Suspension Welds

    Siemens is recalling 35 linear accelerator systems due to defective weld seams that could cause overhead suspensions to fall, posing a risk of severe injury.

    Product
    MEVATRON MD-2, MEVATRON MDX-2 and MEVATRON ME, accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·025-2017·2017-03-15

    RBR Meat Company Recalls Frozen Supreme Pizza Due to Listeria Risk

    RBR Meat Company is recalling approximately 21,220 pounds of frozen Marketside Extra Large Supreme Pizza due to possible Listeria monocytogenes contamination.

    Product
    RBR Meat Co., Inc. — RBR Meat Company, Inc. Recalls Frozen Pizza Product Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1585-2017·2017-03-15

    Versa Marketing Recalls Fusia Szechuan Stir Fry Due to Listeria

    Versa Marketing is recalling Fusia Asian Aspirations Szechuan Stir Fry because the product tested positive for Listeria monocytogenes. The recall affects 4,089 cases sold at Aldi stores nationwide.

    Product
    Fusia Asian Aspirations Szechuan Stir Fry; A delicious blend of premium vegetables with a savory sauce packed in a plastic bag: Sauce packet included. NET WT 21 oz. (1 lb 5 oz) 595 g
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1434-2017·2017-03-15

    Siemens Medical Linear Accelerators Recalled for Defective Weld Seams

    Siemens is recalling 35 MEVATRON M 6730/6740 linear accelerators because defective weld seams on overhead suspensions could break and fall, posing a risk of severe injury.

    Product
    MEVATRON M 6730/6740 (MEX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1435-2017·2017-03-15

    Siemens MEVATRON M 7400/7440 Linear Accelerators Recalled for Defective Welds

    Siemens is recalling 35 MEVATRON M 7400/7440 linear accelerators because a defective weld seam could break, causing the overhead suspension to fall and potentially injure patients or others.

    Product
    MEVATRON M 7400/7440(MEX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1576-2017·2017-03-15

    Stubb's Barbecue Sauce Recalled for Glass Bottle Defects

    McCormick & Co. is voluntarily recalling 18oz bottles of Stubb's Sticky Sweet BBQ Sauce due to glass defects that may cause chipped or missing glass.

    Product
    McCormick & Co., Inc., Stubbs Barbecue. 18oz Best By Date of January 17, 2020.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1581-2017·2017-03-15

    Index Fresh Recalls Hass Avocados Due to Listeria Contamination Risk

    Index Fresh is recalling specific lots of Hass avocados because they may be contaminated with Listeria monocytogenes.

    Product
    Hass Avocado 32 1 Index Fresh- USA Hass Avocado 36 1 Index Fresh- USA Hass Avocado 40 1 Index Fresh- USA Hass Avocado 48 1 Index Fresh- USA Hass Avocado 60 1 Index Fresh- USA Hass Avocado 70 1 Index Fresh- USA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1420-2017·2017-03-15

    Siemens IMMULITE Progesterone Test Kits Recalled for DHEA-S Interference

    Siemens is recalling IMMULITE Progesterone test kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.

    Product
    IMMULITE/ IMMULITE 1000 Progesterone; Catalog Number: LKPW1; Siemens Material Number: 10381128 Product Usage: For in vitro diagnostic use with the IMMULITE¿2000 Systems Analyzers- for the quantitative measurement of progesterone in serum, as an aid in the diagnosis and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V182000·2017-03-15

    Ride The Ducks Recalls Amphibious Vehicles Due to Seat Belt Defect

    Ride The Ducks International LLC is recalling 1996-2014 amphibious vehicles because driver seats and seat belts may not secure occupants in a crash.

    Product
    RIDE THE DUCKS — RIDE THE DUCKS AMPHIBIOUS VEHICLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1583-2017·2017-03-15

    Index Fresh Recalls Hass Avocados Due to Listeria Contamination Risk

    Index Fresh is recalling specific lots of Hass avocados because they may be contaminated with Listeria monocytogenes.

    Product
    Hass Avocado HA LB Signature Farms 15/4 60 1- USA Hass Avocado HA LTP S 60 1 Index Fresh- USA Hass Avocado HA RPCFB 10/4 70 1 Index Fresh- USA Hass Avocado HA LTP 32 2 So Good- USA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1582-2017·2017-03-15

    Index Fresh Recalls Avocados Due to Listeria Contamination Risk

    Index Fresh is recalling 116 cases of Hass avocados distributed in California, Utah, and Washington because they may be contaminated with Listeria monocytogenes.

    Product
    Hass Avocado HA LTP S 40 1 Index Fresh- USA Hass Avocado HA LTP S 70 1 Index Fresh- USA Hass Avocado HA LTP S 70 1 Index Fresh- USA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1399-2017·2017-03-15

    Parker Medical Recalls Left Double Lumen Endobronchial Tubes

    Parker Medical is recalling specific lots of Left Double Lumen Endobronchial Tubes because the single lung isolation feature did not function as intended.

    Product
    Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker Endo-Bronch with Flex Tip). Model Numbers: H-PFTDL-28-1, H-PFTDL-32-1, H-PFTDL-35-1, H-PFTDL-37-1, H-PFTDL-39-1, H-PFTDL-41-1. The product is an endotracheal tube with a double lumen for single lung…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1566-2017·2017-03-15

    Private Selection Salted Caramel Chocolate Almond Pie Recalled for Allergen Mislabeling

    Legendary Baking is recalling Private Selection Salted Caramel Chocolate Almond Pie because the label failed to list eggs and almonds as ingredients.

    Product
    Private Selection, Salted Caramel Chocolate Almond Pie, NET WT 34 OZ ( 2 LB 2 OZ) 963g, UPC 1111054021. Container: In a labeled pie dome and base. Pies are distributed frozen. Some stores sell refrigerated and some sell frozen.
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-1404-2017·2017-03-15

    See Clear Company Recalls Color Contact Lenses for Sterility and Labeling Issues

    The See Clear Company is recalling 119,829 units of color contact lenses because they may not be sterile and may have incorrect lot numbers or expiry dates.

    Product
    Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition, Circle Collection, Lunatic, Fright, Desire and See Clear.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1575-2017·2017-03-15

    Robert Rothschild Farm Recalls Gift Sets with Chocolate Pretzel Dippers

    Robert Rothschild Farm LLC is recalling Gift Sets with Chocolate Pretzel Dippers because the product is not labeled with an ingredient statement, failing to declare the allergens soy and wheat.

    Product
    Gift Sets with Chocolate Pretzel Dippers
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1421-2017·2017-03-15

    Siemens IMMULITE 2000 Progesterone Test Kits Recalled for False Results

    Siemens is recalling IMMULITE 2000 Progesterone kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.

    Product
    IMMULITE 2000 Progesterone; Catalog Number: L2KPW2 L2KPW6; Siemens Material Number: 10381181, 10381170 Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers - for the quantitative measurement of progesterone in serum as an aid in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1427-2017·2017-03-15

    Villa Sistemi Medicali Recalls Juno DRF X-Ray Systems Due to Footrest Detachment

    Villa Sistemi Medicali is recalling 65 Juno DRF x-ray systems because the footrest can detach from the table, causing patients to fall.

    Product
    Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1584-2017·2017-03-15

    Trader Joe's Lemon Curd Recalled for Undeclared Milk Allergen

    Trader Joe's is recalling Imported English Authentic Lemon Curd because it contains undeclared milk in the butter ingredient.

    Product
    Trader Joes Imported English Authentic Lemon Curd, 10.5oz (300g), 24 jars/case
    Category
    Food
    Distribution
    39 states
  • ModerateFDA (Devices)·Z-1411-2017·2017-03-15

    Mako Surgical Recalls MAKO RIO THA Application User Guides

    Mako Surgical Corporation is recalling 777 MAKO RIO THA Application User Guides because five AFMEA Risk Control Measures are missing from the documents.

    Product
    MAKO RIO THA Application User Guides, for total hip arthroplasty, orthopedic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide