The Recall Desk

State

Utah product recalls

73,817 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.

These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42901–42925 of 78733

  • HighFDA (Food)·F-0771-2018·2018-02-14

    Chobani Flip Key Lime Crumble Recalled for Gluten Mislabeling

    Chobani is recalling Flip Key Lime Crumble yogurt because the packaging incorrectly states 'No Gluten' despite containing wheat.

    Product
    Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogurt with Graham Crackers & White Chocolate, 4-packs, 4/5.3 oz cups are packaged with a cardboard overwrap. The net wt. of each single serve up is 5.3 oz. and the net wt. of 4-pack is 21.2 oz. The 4-pack overwrap label…
    Category
    Food
    Distribution
    41 states
  • HighNHTSA·18V108000·2018-02-14

    Toyota Recalls 2018 Camry V6 Vehicles for Fuel Leak Fire Risk

    Toyota is recalling 2018 Camry vehicles with V6 engines because improperly connected fuel pipes may leak fuel, increasing the risk of a fire.

    Product
    TOYOTA — TOYOTA CAMRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0738-2018·2018-02-14

    Wienke's Market Summer Blend Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Summer Blend Jam because it contains butter, an ingredient not listed on the label.

    Product
    Wienke's Market Summer Blend Jam, Packaged in the following sized glass jars: 1. Net Wt. 8 oz (226g), UPC 14106-00237; 2. Net Wt 16 oz UPC 14106-00248. Refrigerate after opening. Ingredients: cherries, strawberries, blackberries, blueberries, red raspberries, sugar…
    Category
    Food
    Distribution
    10 states
  • HighFDA (Drugs)·D-0324-2018·2018-02-14

    Flawless Beauty Recalls Relumins Advanced Glutathione Kits Nationwide

    Flawless Beauty LLC is voluntarily recalling all lots of Relumins Advanced Glutathione kits nationwide because the products were marketed without FDA approval.

    Product
    Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg vials
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0733-2018·2018-02-14

    Wienke's Strawberry Jam Recalled for Undeclared Butter Allergen

    Wienke LLC is recalling Wienke's Market Seedless Strawberry Jam because it contains butter, an ingredient not listed on the label.

    Product
    Wienke's Market Seedless Strawberry Jam, Net Wt. 8 oz (226g), UPC 14106-00232. Refrigerate after opening. Ingredients: strawberry puree, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0514-2018·2018-02-14

    Philips Precedence 16 Imaging System Recalled for Collimator Drop Risk

    Philips is recalling 1,387 Precedence 16 imaging systems because collimators may drop to the floor during exchange, posing a physical hazard.

    Product
    Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Griffin) is an imaging system combining the acquisition of single photon nuclear medicine images and images from an x-ray computed tomography system. Precedence may produce non-attenuation corrected and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0715-2018·2018-02-14

    Wienke's Market Whole Cherry Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market Whole Cherry Jam because it contains butter that is not listed on the label.

    Product
    Wienke's Market Whole Cherry Jam, Net Wt. 8 oz (226g), UPC 14106-00212. Refrigerate after opening. Ingredients: cherries, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-0722-2018·2018-02-14

    Wienke's Market Cranberry Cherry Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Cranberry Cherry Jam because it contains butter, an ingredient not declared on the label.

    Product
    Wienke's Market Cranberry Cherry Jam, Net Wt. 8 oz (226g), UPC 14106-00218. Refrigerate after opening. Ingredients: cranberries, cherries, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-0525-2018·2018-02-14

    ConvaTec Recalls Mislabelled Ostomy Skin Barrier Products

    ConvaTec is recalling a portion of Lot 7H02242 SUR-FIT Natura Moldable Durahesive Skin Barrier units that were incorrectly labeled as Natura Moldable Stomahesive Skin Barrier.

    Product
    SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible Collar, 10 pack, 45 mm, REF 411802. Intended for use as an ostomy protector providing a protective barrier to patient skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0724-2018·2018-02-14

    Wienke's Market Hot Pepper Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market Hot Pepper Jam because it contains butter, an ingredient not declared on the label.

    Product
    Wienke's Market Hot Pepper Jam, Net Wt. 8 oz (226g), UPC 14106-00221. Refrigerate after opening. Ingredients: sweet red peppers, onion, hot peppers, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0711-2018·2018-02-14

    Wienke's Blueberry Rhubarb Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market Blueberry Rhubarb Jam because it contains butter that is not listed on the label.

    Product
    Wienke's Market Blueberry Rhubarb Jam, Net Wt. 8 oz (226g), UPC 14106-00207. Refrigerate after opening. Ingredients: blueberries, rhubarb, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-0548-2018·2018-02-14

    Zimmer Biomet Recalls Humeral Guide Wires Due to Packaging Design Verification Gap

    Zimmer Biomet is recalling 1,517 units of M/DN Intramedullary Fixation Humeral Guide Wires because the previous packaging configuration lacked design verification for 70cm lengths.

    Product
    M/DN Intramedullary Fixation Humeral Guide Wire - Bullet Tip 2.4 mm Diameter 70 cm Length Single Use Only, Item Number 00-2255-026-00 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0543-2018·2018-02-14

    Busse Bone Marrow Biopsy Tray Recalled for Foreign Matter

    Robert Busse & Co. is recalling 5 cases of Safety Deluxe Bone Marrow Biopsy/Aspiration Trays due to the presence of loose polypropylene foreign matter.

    Product
    Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle and Aspiration Needle Sterile, Catalog # 985 Product Usage: Surgical procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0747-2018·2018-02-14

    Wienke's Market Strawberry Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market No Sugar Added Strawberry Jam because it contains butter, an ingredient not listed on the label.

    Product
    Wienke's Market No Sugar Added Strawberry Jam, Net Wt. 8 oz (226g), UPC 14106-00315. Refrigerate after opening. Ingredients: strawberries, rice syrup, grape juice, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-0550-2018·2018-02-14

    Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires

    Zimmer Biomet is recalling 10,116 units of Natural Nail System Tear Drop Guide Wires because the previous packaging configuration lacked design verification for 70cm wires.

    Product
    Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter, 70 cm length, Item Number 47-2490-098-00 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in guiding the nail during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0338-2018·2018-02-14

    McKesson Recalls Subpotent Megestrol Acetate Oral Suspension

    McKesson Packaging Services is recalling Megestrol Acetate Oral Suspension because stability testing found the drug was subpotent.

    Product
    Megestrol Acetate Oral Suspension, USP 400 mg/ 10mL (10 mL UD cups in boxes of 20 cups), Rx Only, Dist. By McKesson Packaging Services a business unit of McKesson Corporation 7101 Weddington Rd. Concord, NC 28027, NDC 63739-549-51
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0548-2018·2018-02-14

    Astellas Recalls Mycamine Injection Vials Due to Labeling Error

    Astellas Pharma US Inc is recalling 63,600 vials of Mycamine (micafungin sodium) for Injection due to a label error on the declared strength.

    Product
    MYCAMINE — MYCAMINE (MICAFUNGIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0529-2018·2018-02-14

    Angiodynamics Recalls Accu2i pMTA Microwave Tissue Ablation Applicators

    Angiodynamics is recalling Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering the desired microwave energy.

    Product
    Accu2i pMTA Applicator, 14 cm STANDARD, REF/Catalog # 900-600-US, Model # (UPN) H787900600US0, STERILE --- This is only for use with a Sulis V Generator, REF 806-10. Product Usage: The Acculis Accu2i pMTA Microwave Tissue Ablation Applicator is indicated for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0551-2018·2018-02-14

    Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires

    Zimmer Biomet is recalling 1,631 units of Natural Nail System Tear Drop Guide Wires because the previous packaging configuration lacked design verification for 70cm wires.

    Product
    Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter, 70 cm length, Item Number 47-2490-098-01 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in guiding the nail during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0721-2018·2018-02-14

    Wienke's Market Currant Jelly Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market Currant Jelly because it contains butter, an ingredient not listed on the label.

    Product
    Wienke's Market Currant Jelly, Net Wt. 8 oz (226g), UPC 14106-00219. Refrigerate after opening. Ingredients: currant juice, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Drugs)·D-0325-2018·2018-02-14

    Flawless Beauty Recalls Relumins Vitamin C Ampules for Misbranding

    Flawless Beauty LLC is voluntarily recalling all lots of Relumins Vitamin C Solvent ampules because they were marketed without an approved NDA or ANDA.

    Product
    Relumins Vitamin C Solvent ampules
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0552-2018·2018-02-14

    3M Recalls ACE Ultra Lite Ankle Braces Due to Mold Contamination

    3M is recalling specific sizes of ACE Ultra Lite Ankle Braces because mold was found on non-patient contact surfaces. The mold was identified as Aspergillus candidus.

    Product
    ACE(TM) BRAND, ULTRA LITE ANKLE brace: (a) Size Selection Medium, Cat #901014, UPC 051131019984 2; (b) Size Selection Large, Cat #901015, UPC 0 51131019985 9
    Category
    Medical Device
    Distribution
    32 states
  • ModerateFDA (Drugs)·D-0327-2018·2018-02-14

    Flawless Beauty Recalls Laroscorbine Platinum Vitamin C Due to Misbranding

    Flawless Beauty LLC is voluntarily recalling all lots of Laroscorbine Platinum Vitamin C products because they were marketed without an approved NDA or ANDA.

    Product
    Laroscorbine Platinum Vitamin C 1 gm Collagen 0.35 gm, Roche
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0542-2018·2018-02-14

    Busse Lumbar Puncture Tray Recalled for Foreign Matter

    Busse Hospital Disposables is recalling Safety-Deluxe Lumbar Puncture Trays because they may contain loose polypropylene foreign matter above release specifications.

    Product
    Safety-Deluxe Lumbar Puncture Tray, Catalog # 975 Product Usage: Surgical procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0739-2018·2018-02-14

    Wienke's Apple Butter Recalled for Undeclared Butter Ingredient

    Wienke LLC is recalling No Sugar Added Apple Butter because it contains butter, an ingredient not listed on the label.

    Product
    Wienke's Market No Sugar Added Apple Butter, Net Wt. 8 oz (226g), UPC 14106-00300. Refrigerate after opening. Ingredients: apples, cinnamon, cloves, allspice.
    Category
    Food
    Distribution
    10 states