The Recall Desk

State

Utah product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35726–35750 of 78722

  • HighFDA (Devices)·Z-1778-2019·2019-06-19

    Getinge 86-Series Medical Washer-Disinfector Recalled for Potential Hose Collapse

    Maquet Cardiovascular is recalling 40 Getinge 86-Series Medical Washer-Disinfector units because the inlet pump hose may collapse, potentially preventing proper cleaning of medical instruments.

    Product
    Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product Usage: The Getinge 86 Series Medical Washer-Disinfector is designed for use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia sets, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1452-2019·2019-06-19

    Meiji Chocolate Macadamia Bars Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Macadamia bars because they lack English labels for nutrition facts, ingredients, and allergens.

    Product
    CHOCOLATE MACADAMIA MEIJI, 2.25 oz. Item number 69920 UPC 074410699208 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1777-2019·2019-06-19

    Getinge 86-Series Medical Washer-Disinfector Recalled for Potential Hose Collapse

    Maquet Cardiovascular is recalling four Getinge 86-Series Medical Washer-Disinfector units because the inlet pump hose may collapse, potentially preventing proper cleaning of medical instruments.

    Product
    Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product Usage: Usage: The Getinge 86 Series Medical Washer-Disinfector is designed for use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia sets…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1769-2019·2019-06-19

    Terumo Electronic Patient Gas System Recalled for Control Slider Failure

    Terumo is recalling 72 Electronic Patient Gas Systems used in cardio-pulmonary bypass because a fault disables control sliders, forcing use of local knobs.

    Product
    Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI 00886799000588. Used in cardio-pulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19E041000·2019-06-19

    Gillig Recalls Transpec T287X Series Glass Roof Hatches for Shattering Risk

    Gillig LLC is recalling Transpec T287X Series glass roof hatches sold as aftermarket parts because temperature and vibration stresses may cause the tempered glass to shatter, potentially injuring passengers.

    Product
    STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1454-2019·2019-06-19

    Meiji Chocolate Wheat Snack Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Takenoko no Sato bars because they lack English labels for ingredients and allergens, including milk, soy, egg, and tree nuts.

    Product
    CHOCOLATE TAKENOKO NO SATO MEIJI (Chocolate wheat snack, 2.46 oz. Item number 65880 UPC 074410658809 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·19V474000·2019-06-19

    Audi Recalls Vehicles Due to Passenger Air Bag Deactivation Risk

    Audi is recalling specific 2015-2019 models because an electrical issue may cause the passenger air bag to deactivate, increasing injury risk in a crash.

    Product
    AUDI — AUDI A3 CABRIOLET, RS 3, A3 SPORTBACK E-TRON, S3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1453-2019·2019-06-19

    Meiji Chocolate Kinoko No Yama Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Kinoko No Yama bars because they lack English labels for ingredients and allergens.

    Product
    CHOCOLATE KINOKO NO YAMA MEIJI, 2.61 oz. Item number 65879 UPC 074410658793 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-1399-2019·2019-06-19

    Synthetopes Recalls Pentreotide Vials Due to Lack of Processing Controls

    Synthetopes Inc. is recalling Pentreotide (10 uGm) vials nationwide due to a lack of processing controls. All lots remaining within expiry are affected.

    Product
    Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1342-2019·2019-06-19

    Chiesi Recalls Zileuton Extended-Release Tablets Due to Dissolution Failure

    Chiesi USA is recalling 2,598 bottles of Zileuton Extended-Release Tablets, 600 mg, because they failed dissolution specifications.

    Product
    Zileuton Extended-Release Tablets, 600 mg, 120-count bottles, Rx only, Distributed by: Prasco Laboratories, Mason, OH 45040 USA; NDC 66993-485-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1751-2019·2019-06-19

    GE Healthcare Recalls Prestige Systems Due to Monitor Mount Failure

    GE Healthcare is recalling Prestige II, SI, and VH systems because a CRT monitor fell off its wall mount due to product aging.

    Product
    Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote controlled system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1436-2019·2019-06-19

    Geritrex Recalls Senna Syrup Due to Atypical Odor and Taste

    Geritrex, LLC is recalling 1,536 bottles of Senna Syrup due to reports of atypical odor and unpleasant taste.

    Product
    Senna (sennosides 8.8 mg) Syrup, 8 fl oz. (237 mL) bottles, Rij Pharmaceuticals Corporation 40 Commercial Avenue, Middletown, NY 10941, NDC 53807-556-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1341-2019·2019-06-19

    Chiesi Recalls ZYFLO CR Tablets Due to Dissolution Failure

    Chiesi USA is recalling ZYFLO CR (zileuton) extended-release tablets because they failed to meet dissolution specifications. The recall affects 2,118 bottles distributed nationwide.

    Product
    ZYFLO CR (zileuton) extended-release tablets, 600 mg, 120-count bottles, Rx only, Distributed by Chiesi USA, Inc., Cary, NC 27518, NDC 10122-902-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1754-2019·2019-06-19

    GE Healthcare Precision 500D X-ray System Recall for Monitor Mount Failure

    GE Healthcare is recalling Precision 500D X-ray systems because a CRT monitor fell off its wall mount due to product aging.

    Product
    Precision 500D The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and pediatric examinations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1401-2019·2019-06-19

    Synthetopes Recalls Sn-Mertiatide Kit Due to Processing Control Deficiencies

    Synthetopes Inc is recalling Sn-Mertiatide Kits nationwide due to a lack of processing controls. The recall covers all lots remaining within their expiry date.

    Product
    Sn-Mertiatide Kit,1 milligram betiatide, Not for Direct Injection, Store at Room Temperature, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1449-2019·2019-06-19

    Meiji Chocolate Milk Chocolate Bars Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Milk Chocolate bars because they lack English labels for ingredients and allergens, including milk, soy, egg, and tree nuts.

    Product
    CHOCOLATE MILK CHOCOLATE MEIJI, 1.75 oz. Item number 70378 UPC 074410703783 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-1451-2019·2019-06-19

    Meiji Chocolate Almond Bars Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Almond bars because they lack English labels for ingredients and allergens, including milk, soy, egg, and tree nuts.

    Product
    CHOCOLATE ALMOND CHOCOLATE MEIJI, 3.1 oz. Item number 64344 UPC 074410643447 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-1437-2019·2019-06-19

    Geritrex Recalls Senna Syrup Due to Atypical Odor and Taste

    Geritrex, LLC is recalling Senna Syrup bottles due to reports of atypical odor and unpleasant taste.

    Product
    Senna (sennosides 8.8 mg) Syrup 8 fl oz. (236 mL) bottles, Distributed by Geritrex, LLC 40 Commercial Avenue Middletown, NY 10941, NDC 54162-007-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1450-2019·2019-06-19

    Meiji Black Chocolate Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Black Chocolate bars because they lack English labels for nutrition facts, ingredients, and allergens.

    Product
    CHOCOLATE BLACK CHOCOLATE MEIJI, 1.75 oz. Item number 69341 UPC 074410693411 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-1340-2019·2019-06-19

    Glenmark Recalls Estradiol Vaginal Inserts Due to Defective Plunger

    Glenmark Pharmaceuticals is recalling Estradiol Vaginal Inserts because the plunger delivery system is not functioning properly.

    Product
    ESTRADIOL VAGINAL INSERTS — ESTRADIOL VAGINAL INSERTS (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1773-2019·2019-06-19

    CardioCommand Transesophageal Cardiac Pacing System Recalled for Battery Corrosion

    Cardiocommand Inc. is recalling five units of its Transesophageal Cardiac Pacing and Recording System, Model 7A, due to possible corrosion of the battery contacts.

    Product
    CardioCommand, Inc. Transesophageal Cardiac Pacing and Recording System, Model 7A, REF 0101 - Product Usage: Indications for Use: - Temporary left atrial pacing to treat bradycardia, hypotension or AV junctional rhythm - Acceleration of heart rate as an alternative to exercise…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1455-2019·2019-06-19

    Meiji Chocolate Choco Baby Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Choco Baby bars because they lack English labels for nutrition facts, ingredients, and allergens.

    Product
    CHOCOLATE CHOCO BABY (S) MEIJI, 1.19 oz. Item number 70582 UPC 074410705824 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1776-2019·2019-06-19

    Conformis iTotal Hip Replacement System Recalled for Dimensional Discrepancy

    Conformis is recalling 183 iTotal Hip Replacement System stems nationwide due to a 3mm discrepancy between approved and manufactured neck/head lengths.

    Product
    Conformis iTotal Hip Replacement System: HBS-033-00xx-020101, (HIP-PATIENT SPECIFIC STEM RIGHT)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1402-2019·2019-06-19

    Synthetopes Recalls Sulfur Colloid Reaction Vials Due to Processing Controls

    Synthetopes Inc. is recalling Sulfur Colloid Reaction Vials nationwide due to a lack of processing controls.

    Product
    Sulfur Colloid Reaction Vial 1.0 mL, Thaw Before Use, Not for Direct Injection, Store Frozen, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide