The Recall Desk

State

Utah product recalls

20,304 recalls have nationwide distribution and so reach Utah. 0 additional recalls listed Utah specifically in their distribution scope.

About recalls in Utah

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Utah consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

11701–11725 of 20304

  • HighFDA (Food)·F-1505-2023·2023-09-20

    Twin City Foods Frozen Corn Recalled for Listeria Contamination Risk

    Multiple frozen corn products distributed nationwide are being recalled due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.

    Product
    Kernel Corn, BEST PRICE TOPVALU, net wt. per bag 300g. Label is in foreign language. UPC 4549414086232 Signature Select Golden Corn Super Sweet, Product of USA, net wt. per bag 12oz, 12 bags per case. UPC 21130090655 Food Lion Super Sweet Cut Yellow Corn, Product of USA, net wt
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1503-2023·2023-09-20

    Twin City Foods Frozen Corn Recalled Nationwide for Listeria Risk

    Twin City Foods recalled frozen corn products due to potential Listeria monocytogenes contamination. Products distributed nationwide and internationally.

    Product
    Individually Quick Frozen (IQF) Corn distributed in BULK TOTES (1650lbs and 1750lbs) to consignees for further processing. Bulk tote labels have cooking instructions. Individually Quick Frozen (IQF) Super Sweet Corn, foodservice item, packaged in 32oz. plastic bag, 12 bags per
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2577-2023·2023-09-20

    BeamAdjust software generates incorrect calibration files for radiation detectors

    BeamAdjust software Version 2.3.3 generates incorrect calibration files when using TIFF or DICOM image reference data, affecting radiation measurement accuracy in OCTAVIUS Detector systems.

    Product
    BeamAdjust software Version 2.3.3 Ref: S080032 The following devices are affected when a relative calibration is performed using ArrayCal (module from BeamAdjust S080032, UDI-DI: EPTWS0800320 ): " OCTAVIUS Detector 1600 SRS (T10056) (UDI-DI: EPTWT100560) " OCTAVIUS Detector
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1504-2023·2023-09-20

    Frozen Corn Recalled Due to Listeria monocytogenes Contamination

    Twin City Foods frozen corn in bulk cases is recalled nationwide due to potential Listeria monocytogenes contamination. Products were distributed to food processors in the United States, Costa Rica, China, and Japan.

    Product
    Individually Quick Frozen (IQF) Corn, distributed in bulk cases (1kg, 10kg, 12kg, 15kg, 25kg) to consignees for further processing. Cases are read in parts: Product of U.S.A. Packed By Twin City Foods, Inc. Stanwood, Washington. Super Sweet Grade A Cut Corn Blanched Vegetables,
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2581-2023·2023-09-20

    Welch Allyn Connex Spot Monitor Recalled for Improper Copper Tape Placement

    Baxter Healthcare is recalling the Welch Allyn Connex Spot Monitor due to improper placement of copper tape on the back of the liquid-crystal display. The device was distributed in California.

    Product
    Welch Allyn Connex Spot Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2576-2023·2023-09-20

    Microbiologics KWIK-STIK ANA quality control set missing strain

    Microbiologics Inc is recalling one lot of KWIK-STIK ANA QC sets missing one of three bacterial strains required for microbiological testing.

    Product
    KWIK-STIK, ANA (3 Strains) QC Set, REF 5065P; Microbiological testing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2579-2023·2023-09-20

    Copaliner Cavity Varnish Recalled for Solvent Mislabeling Error

    Keystone Industries recalls Copaliner Cavity Varnish after discovering bottles of Copaliner Solvent were accidentally packaged in boxes labeled as varnish. The error affected 337 units distributed worldwide.

    Product
    Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to provide a marginal seal between the dentin and amalgam which helps to protect against penetration of amalgam into the dentina Item No. 0921526
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2580-2023·2023-09-20

    Denture relining kit recalled for outer box labeling error

    Keystone Industries is recalling 240 units of Henry Schein Hard Line Chairside Reline kits because the outer box is labeled as Soft Line, though the contents and instructions are correctly labeled.

    Product
    Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture Relining Material KI Item No.: 0921940HS Henry Schein Item No.: 570-0718
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·23286·2023-09-14

    Chuckle & Roar Ultimate Water Beads Activity Kits Recalled for Ingestion and Choking Hazards

    Buffalo Games and Target are recalling Chuckle & Roar Ultimate Water Beads Activity Kits because ingested water beads expand and can cause choking and intestinal obstruction in children. One infant death and one serious injury requiring surgery have been reported.

    Product
    Chuckle & Roar Ultimate Water Beads Activity Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23288·2023-09-14

    Generac Portable Generators Recalled for Fire and Burn Hazards

    Generac is recalling about 64,000 portable generators because the fuel tank can fail to vent properly, causing excess pressure and fuel expulsion that poses fire and burn hazards. Generac has received 27 incident reports, including three with severe burn injuries.

    Product
    Generac Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23792·2023-09-14

    Best Buy Insignia and Yardbird Fire Tables Recalled for Burn and Impact Injury Hazards

    Best Buy is recalling approximately 1,490 Insignia and Yardbird fire tables with lava rocks because the lava rocks can split and eject, posing burn and impact injury hazards. Consumers should immediately stop using the recalled fire tables.

    Product
    Insignia and Yardbird fire tables with lava rocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23287·2023-09-14

    Honda Lawnmowers and Pressure Washer Engines Recall Due to Starter Rope Injury Hazard

    American Honda is recalling about 391,800 lawnmowers and pressure washer engines because improperly manufactured camshafts can cause the starter rope to suddenly retract when pulled, posing an injury hazard. The company has received 2,197 reports of incidents, including seven minor injuries.

    Product
    Honda Lawnmowers and Pressure Washer Engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23282·2023-09-14

    STIHL MSA 300 Battery-Powered Chain Saws Recalled for Slow Braking

    STIHL Incorporated is recalling about 2,800 MSA 300 battery-powered chain saws because the braking system can take longer to brake than expected, creating a laceration hazard. Consumers should stop using the product immediately and contact an authorized dealer for a free replacement of the brake drum and brake band.

    Product
    STIHL MSA 300 chain saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23280·2023-09-14

    Foldable Bistro Set Chairs Recalled Due to Fall Hazard

    TJX is recalling about 11,000 foldable bistro set chairs sold at Marshalls, T.J. Maxx, HomeGoods, and Homesense stores because the wooden frame can break or collapse when someone sits in it, causing falls. The firm has received seven reports of frame failure, including four involving minor injuries.

    Product
    Foldable Bistro Set Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1169-2023·2023-09-13

    Digoxin Tablets Nationwide Recall: Bottles Mislabeled with Incorrect Dosages

    Marlex Pharmaceuticals recalls Digoxin Tablets nationwide due to a labeling error where bottles are mislabeled with incorrect dosages. Bottles labeled as 0.125mg contain 0.25mg and vice versa.

    Product
    Digoxin Tablets, USP 0.125mg, 100-count bottles, Rx Only, Manufactured for/Distributed by: Marlex Pharmaceuticals, Inc. New Castle, DE NDC# 10135-0747-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2519-2023·2023-09-13

    Hip Prosthesis Implants Recalled for Size Mismatch Between Label and Device

    Zimmer, Inc. is recalling M/L Taper Hip Prosthesis implants where the outer package labeling and product etch do not match the actual implant size. This mislabeling could lead to implantation of the wrong-sized prosthesis.

    Product
    M/L Taper Hip Prosthesis Extended Offset, Reduced Neck Length, Size 4 (Item Number 00771100640) and Size 6 (Item Number 00771100440)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2516-2023·2023-09-13

    Fargo Ortho-K Contact Lens Recall Due to Missing FDA Approval

    PARAGON VISION SCIENCES is recalling 18,820 Fargo Ortho-K contact lenses because they were manufactured without required FDA approval. Patients should contact their eye care provider.

    Product
    Fargo Ortho-K Lens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2522-2023·2023-09-13

    Olympus Distal Attachment Recalled for Phthalate Exceeding Permissible Levels

    Aomori Olympus Co., Ltd. recalls 1,048 Olympus Distal Attachment units used in EMR kits due to di-2-ethylhexyl phthalate (DEHP) exceeding permissible exposure limits per ISO 10993-17: 2002. Devices were distributed nationwide.

    Product
    Olympus Distal Attachment (in Olympus Disposable EMR Kit)- Designed to be attached to the distal end of the endoscope. Disposable EMR Kit: K-001, K-002, K-003, K-004, K-011, K-012
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2523-2023·2023-09-13

    Reusable Endoscopy Distal Attachments Recalled for Excessive DEHP Levels

    Aomori Olympus recalls 1,252 reusable distal attachment devices with DEHP chemical levels exceeding safe exposure limits per medical device standards. Devices distributed nationwide in the United States.

    Product
    Reusable distal attachments Models: MH-462, MH-463, MH-464, MH-465, MH-466, MH-483, MH-587, MH-588(US), MH-589, MH-590, MH-591, MH-592, MH-593, MH-594, MH-595, MH-596, MH-597, MH-598, MAJ-289, MAJ-290, MAJ-291, MAJ-292, MAJ-293, MAJ-294, MAJ-295, MAJ-296, MAJ-297, MAJ-663, MAJ-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2513-2023·2023-09-13

    Cook Lead Clipper Cardiac Device Sterility Recall Due to Packaging Defect

    Cook Vandergrift is recalling approximately 15,951 Cook Lead Clipper devices due to potential sterility compromise from packaging seal breaches. The surgical tool is used for cardiac lead retrieval procedures.

    Product
    Cook Lead Clipper- An auxiliary tool indicated for use in patients requiring percutaneous retrieval of cardiac leads. Order Number (GPN): G20003 Reference Part Number (RPN): LR-CLP001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2518-2023·2023-09-13

    Trocar with oversized shaft obscures surgical view in brain operations

    Aesculap trocars manufactured with shafts too long obstruct the visual field when used with neuroendoscopes in brain surgery. Affected units distributed in nine states should not be used.

    Product
    For intraventricular indications mainly used for operations within the brain ventricles. Product Code: FF399R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2404-2023·2023-09-13

    Medical Imaging System Recalled for Foot Pedal Malfunction Risk

    Philips MultiDiagnost-Eleva imaging systems may emit unintended radiation if the foot pedal gets stuck in the active position. The FDA is alerting healthcare facilities to this potential equipment malfunction.

    Product
    MultiDiagnost-Eleva
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2517-2023·2023-09-13

    Philips 3D9-3v Ultrasound Transducer may separate due to bonding defect

    Philips 3D9-3v Transducer units may separate at the chassis bonding, risking electric shock and tissue damage if safety systems fail. Affected units distributed worldwide.

    Product
    3D9-3v Transducer, accessory to Philips Ultrasound Systems: EPIQ Elite; Affiniti 30, 50, and 70; ClearVue 850; HD15; iU22; and Compact 5000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2403-2023·2023-09-13

    Azurion imaging systems recalled for stuck foot switch causing unintended radiation

    Philips recalls Azurion imaging systems because the foot switch pedal may stick in the active position, causing unintended radiation emission. Facilities should stop using the systems and contact Philips for guidance.

    Product
    Azurion
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1170-2023·2023-09-13

    Digoxin Tablets Recalled Due to Reversed Dosage Labeling

    Marlex Pharmaceuticals is recalling Digoxin Tablets because bottles labeled as 0.125mg contain 0.25mg strength, and vice versa. Approximately 94 100-count bottles distributed nationwide are affected.

    Product
    Digoxin Tablets, USP 0.25mg, 100-count bottles, Rx Only, Manufactured for/Distributed by: Marlex Pharmaceuticals, Inc. New Castle, DE NDC 10135-0748-01
    Category
    Drug
    Distribution
    Distributed nationwide