The Recall Desk

State

Kentucky product recalls

72,986 recalls have nationwide distribution and so reach Kentucky. 7,165 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total
7,165
Critical
1,399
Severe
1,694
Most recent
2026-09-09

Of the 7,165 recalls naming Kentucky we have scored against our rubric, 1,399 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,694 (24%) are Severe.

These figures cover only the 7,165 recalls whose distribution notice names Kentucky specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6401–6425 of 80151

  • HighNHTSA·25V430000·2025-06-26

    Jeep Grand Cherokee blower motor failure can disable windshield defrosting

    Chrysler is recalling certain 2023 Jeep Grand Cherokee and Grand Cherokee L vehicles because the blower motor may fail, leaving the defrosting and defogging system inoperative. This fails FMVSS 103.

    Product
    JEEP — JEEP GRAND CHEROKEE L, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V436000·2025-06-26

    Kenworth and Peterbilt trucks with lighting and axle control defect

    PACCAR is recalling 2024–2026 Kenworth and Peterbilt trucks. A software fault may prevent tail brake lights, headlights, reverse lights, and turn signals from illuminating properly, and may cause lift axles to unexpectedly raise or oscillate.

    Product
    PETERBILT — PETERBILT, KENWORTH 589, T480, T180, T280
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V429000·2025-06-26

    Great Dane Recalls 2026 Champion Trailers Due to Door Bolt Issue

    Great Dane is recalling 2026 Champion dry van trailers because roll-up door operator bolts may not be tightened, increasing the risk of injury.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25358·2025-06-26

    Professional's Choice Equine Swivel Port Bits Recalled for Fall Hazard

    Professional's Choice Sports Medicine Products is recalling Swivel Port equine bits from the Bob Avila collection because the bits can break during use, posing a fall hazard to riders. The company has received five reports of bits breaking but no injuries have been reported.

    Product
    Swivel Port equine bits from Bob Avila collection
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1944-2025·2025-06-25

    Dexcom G7 Glucose Receiver recalled due to defective foam or assembly error

    Dexcom, Inc. is recalling Dexcom G7 Glucose Receiver units due to defective foam or assembly error that may cause the speaker to lose contact with the circuit board, preventing audible alerts for low or high blood glucose.

    Product
    Dexcom G7 Glucose Receiver, SKUs (part number): STK-AT-011(MT26403-0), STK-AT-012 (MT26403-0), STK-AT-013 (MT26403-0), STK-GT-001 (MT26403-1), STK-GT-008 (MT26403-5), STK-GT-013 (MT26403-1) , STK-GT-019 (MT26403-4) , STK-GT-100 (MT26403-2), STK-GT-109 (MT26403-2) , STK-GT-113 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1945-2025·2025-06-25

    Dexcom One+ Continuous Glucose Monitoring System Receiver Speaker Defect

    Dexcom, Inc. is recalling 26,291 units of the Dexcom One+ Continuous Glucose Monitoring System due to defective foam or assembly errors that may prevent audible alerts for low or high blood glucose levels, potentially leading to seizures, loss of consciousness, or death.

    Product
    Dexcom One+ Continuous Glucose Monitoring System, SKU(Part Number): STK-D7-013 (MT28285-1), STK-D7-014 (MT28285-1), STK-D7-103 (MT28285-2)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1946-2025·2025-06-25

    Dexcom One Continuous Glucose Monitoring System Receiver Speaker Defect

    Dexcom, Inc. is recalling Dexcom One Continuous Glucose Monitoring System receivers due to potential defective foam or assembly errors that may cause the speaker to lose contact with internal components, resulting in missed audible alerts for dangerous blood glucose levels.

    Product
    Dexcom One Continuous Glucose Monitoring System, SKUs(Part Number): STK-DO-006 (MT27409-1), STK-DO-013 (MT27409-1), STK-DO-103 (MT27409-2), STK-DO-109 (MT27409-2)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1943-2025·2025-06-25

    Dexcom G6 Glucose Receiver recalled for missed audible alerts

    Dexcom G6 Glucose Receiver units may have defective foam or assembly errors that disable audible alerts for dangerously low or high blood glucose, risking seizures, loss of consciousness, or death.

    Product
    Dexcom G6 Glucose Receiver, SKUs (Part Number): STK-FM-001 (MT27408-1) & STK-FR-001 (MT27408-1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0054-2025·2025-06-25

    Ready-to-eat salads recalled for potential Salmonella contamination

    GBC Food Services is recalling multiple ready-to-eat salad products due to potential Salmonella contamination. The affected salads were purchased between May 8 and May 21, 2025.

    Product
    Chef Salad 11oz 850065403328 Purchase Dates: 05/08/2025 to 05/21/2025 Family Cobb Salad 22OZ 850054894625 Purchase Dates: 05/08/2025 to 05/21/2025 Individual Garden Salad 12OZ 850054894618 Purchase Dates: 05/08/2025 to 05/21/2025 Individual Greek Salad 12OZ 850054894649 Purchase
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·H-0052-2025·2025-06-25

    Cucumber bowls and snack cups recalled due to Salmonella contamination risk

    GBC Food Services, LLC is recalling cucumber products sold between May 8 and May 21, 2025, due to potential Salmonella contamination. Affected products include Cucumber Bowl with Ranch dip, Cucumber Slices with Tajin, and Cucumber with Ranch Snack Cup.

    Product
    Cucumber Bowl with Ranch dip 15oz UPC 850054894519 Purchase Dates: 05/08/2025 to 05/21/2025 Cucumber Slices W/Tajin 10 oz UPC 85005368569 Purchase Dates: 05/08/2025 to 05/21/2025 Cucumber w/ Ranch Snack Cup 9.5 oz UPC 850065403144 Purchase Dates: 05/08/2025 to 05
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Drugs)·D-0492-2025·2025-06-25

    UNAVY ACIDO HIALURONICO supplement recalled for undeclared pharmaceutical ingredients

    UNAVY ACIDO HIALURONICO hyaluronic acid supplement is being recalled because it contains three undeclared pharmaceutical ingredients: Dexamethasone, Diclofenac, and Omeprazole. The product was marketed without FDA approval and poses health risks from the unlisted drugs.

    Product
    UNAVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7 503046 054295
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V414000·2025-06-25

    International CV brake pressure sensor can leak fluid causing fire

    International is recalling certain 2019-2025 CV vehicles because the brake pressure sensor assembly may leak brake fluid into the pressure switch and short circuit. Owners are advised to park outside until repaired.

    Product
    INTERNATIONAL — INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0053-2025·2025-06-25

    Vegetable Bowls and Trays Recalled for Potential Salmonella Contamination

    GBC Food Services is recalling vegetable bowls and vegetable ranch trays due to potential Salmonella contamination. Affected products were purchased between May 8 and May 21, 2025.

    Product
    Vegetable Bowl $5 13oz 850065403380 Purchase Dates: 05/08/2025 to 05/21/2025 Vegetable Bowl $10 26 oz 860010507131 Purchase Dates: 05/08/2025 to 05/21/2025 Vegetable Ranch Tray No Dip Small 19.50 oz 850054894335 Purchase Dates: 05/08/2025 to 05/21/2025 Large Vegetable Tray
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Drugs)·D-0493-2025·2025-06-25

    UMOVY ACIDO HIALURONICO supplement recalled for undeclared prescription drugs

    UMOVY ACIDO HIALURONICO dietary supplement has been recalled because it contains undeclared prescription ingredients Dexamethasone and Diclofenac. The product was marketed without FDA approval.

    Product
    UMOVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7503046054134
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V433000·2025-06-25

    Chevrolet Blazer EV parking brake wiring can trigger or lose the brake

    General Motors is recalling certain 2024-2025 Chevrolet Blazer EV vehicles because a damaged or corroded rear parking brake harness can activate the parking brake while driving, or disable it while parked.

    Product
    CHEVROLET — CHEVROLET BLAZER EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·021-2025-EXP·2025-06-25

    Starway Recalls Ineligible Frozen Siluriformes Fish Products Imported from Vietnam

    Starway International Group is expanding a recall for frozen fish products from an ineligible Vietnamese establishment. No adverse reactions have been reported.

    Product
    Starway International Group LLC Expands Recall for Ineligible Frozen Siluriformes Fish Products Imported from Vietnam
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0056-2025·2025-06-25

    Cucumber Carrot Ranch Pack 20oz recalled for Salmonella contamination

    GBC Food Services is recalling Cucumber Carrot Ranch Pack 20oz due to potential Salmonella contamination. The affected products were purchased between May 8 and May 21, 2025, and distributed across nine states.

    Product
    Cucumber Carrot Ranch Pack 20oz 850065403557 Purchase Dates: 05/08/2025 to 05/21/2025
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0055-2025·2025-06-25

    Fruit and Veg Tray 64oz Recalled for Potential Salmonella Contamination

    GBC Food Services, LLC is recalling Fruit and Veg Tray 64oz products due to potential Salmonella contamination. The affected products were distributed to multiple states and purchased between May 8 and May 21, 2025.

    Product
    Fruit and Veg Tray 64oz 850065403748 Purchase Dates: 05/08/2025 to 05/21/2025
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-1987-2025·2025-06-25

    Biomet 3i Certain-Compatible 4.1mm Milled Titanium Dental Abutments

    Preat Corp is recalling Biomet 3i Certain-compatible 4.1mm Milled Titanium Abutments (Model 9001767-F) due to manufacturing defects that may cause improper screw engagement. The screw seat was positioned too high, potentially compromising the attachment of mating screws to the underlying implant.

    Product
    Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1980-2025·2025-06-25

    Portable Oxygen Concentrator with Erroneous Calibration Values

    Ohio Medical Corporation is recalling 36 units of the GCE HEALTHCARE Zen-O lite portable oxygen concentrator due to erroneous calibration values that may cause the device's alarm for low oxygen purity to function incorrectly as the device ages.

    Product
    GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1982-2025·2025-06-25

    Siemens UROSKOP Omnia Max frequency inverter fire risk recalled

    Siemens is recalling UROSKOP Omnia Max medical devices due to a resistor in the frequency inverter that may overheat and ignite the plastic housing. Twenty-five units distributed nationwide are affected.

    Product
    UROSKOP Omnia Max. Model Number: 10762473
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1981-2025·2025-06-25

    UROSKOP Omnia X-ray System Model 10094910 Frequency Inverter Overheating Recall

    Siemens is recalling 95 units of the UROSKOP Omnia X-ray system nationwide due to a resistor in the frequency inverter that may overheat and potentially ignite the plastic housing.

    Product
    UROSKOP Omnia. Model Number: 10094910
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1992-2025·2025-06-25

    Fresenius 5008X HDF Hemodialysis Blood Tubing Sets recalled for potential blood leaks

    Fresenius Medical Care is recalling 5008X HDF Hemodialysis Blood Tubing Sets due to potential blood leaks between the venous chamber and tubing. The recall affects hemodialysis, hemodiafiltration, hemofiltration, and isolated ultrafiltration procedures nationwide.

    Product
    5008X HDF Hemodialysis Blood Tubing Set, 24 units per case, with the following models: a. 5008X Standard HDF Bloodline, Model Number: 03-5100-7. b. 5008X Standard HDF Bloodline w/CLIC, Model Number: 03-5100-7C. c. 5008X Standard HDF Bloodline w/ Twister, Model Number: 03-5150-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1990-2025·2025-06-25

    ICU Medical Plum Duo Infusion Pump Software Dose Limit Issue

    ICU Medical is recalling Plum Duo infusion pumps with software version 1.1.1 because a workflow may bypass the Maximum Dose Limit alert, potentially allowing unsafe medication doses to be programmed.

    Product
    ICU Medical Plum Duo, Item numbers: 1) 400020401, 2) 400021001 , and 3) 400021003; infusion pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1991-2025·2025-06-25

    ICU Medical Plum Solos Infusion Pump Software Safety Defect Recall

    ICU Medical is recalling Plum Solos infusion pumps (Item 400011001) with software version 1.1.1 due to a workflow that may bypass the Maximum Dose Limit alert, which is designed to prevent overdose. The defect affects 214 units distributed across nine US states and the Philippines.

    Product
    ICU Medical Plum Solos, Item number 400011001; infusion pump
    Category
    Medical Device
    Distribution
    Distributed nationwide