The Recall Desk

State

Kentucky product recalls

73,576 recalls have nationwide distribution and so reach Kentucky. 7,203 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total
7,203
Critical
1,409
Severe
2,024
Most recent
2026-10-21

Of the 7,203 recalls naming Kentucky we have scored against our rubric, 1,409 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,024 (28%) are Severe.

Which agencies issued them

These figures cover only the 7,203 recalls whose distribution notice names Kentucky specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26376–26400 of 80779

  • HighFDA (Food)·F-0777-2021·2021-07-21

    Living Free Heart/Blood Vessel Dietary Supplement Recalls for Undeclared Soy

    Bea Lydeckers Naturals Inc is recalling Living Free Heart/Blood Vessel Dietary Supplement because the label declares lecithin but does not declare that it is soy lecithin, posing a risk to consumers with soy allergies.

    Product
    Living Free Heart/Blood Vessel Dietary Supplement, 100 or 500 capsules per bottle. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Heart/Blood Vessel Dietary Supplement***Glandular Herbal & Vitamin…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0778-2021·2021-07-21

    Living Free Immune Dietary Supplement Soy Allergen Mislabeling Recall

    Bea Lydeckers Naturals Inc is recalling Living Free Immune Dietary Supplement because the label declares lecithin but does not declare that it contains soy lecithin, posing a risk to consumers with soy allergies.

    Product
    Living Free Immune Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Immune Dietary Supplement***Glandular and Herbal Supplement***Formulated by Beatrice…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2070-2021·2021-07-21

    Arrow Bipolar Balloon Electrode Catheter Recalled for Marketing Without FDA 510K Clearance

    Arrow International is recalling 4 units of an electrode catheter marketed without FDA 510(k) clearance. The device was intended for electrophysiology studies.

    Product
    Arrow Bipolar Balloon Electrode Catheter 5 Fr. 105 cm, Product Code: AI-07154 - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2046-2021·2021-07-21

    Canon MRI System Recalled for Flame-Retardancy Component Defect

    Canon Medical System recalled its Vantage Titan 3T MRI systems due to a component lacking proper flame-retardancy standards. The defect could produce smoke or fire during use.

    Product
    Canon Vantage Titan 3T, Premium Open-Bore MRI System, REF: MRT-3010 - Product Usage: use as a diagnostic imaging modality that produces cross-sectional transaxial, coronal, sagittal, and oblique images that display anatomic structures of the head or body. Additionally, this…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V552000·2021-07-21

    Kalmar Recalls 2021 Ottawa T2 Vehicles Due to Stability Control Defect

    Kalmar is recalling 2021 Ottawa T2 vehicles because an incorrectly installed rear stability control harness may cause the system to be inactive, increasing crash risk.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0779-2021·2021-07-21

    Living Free Lung & Joint Congestion Herbal Dietary Supplement Soy Allergen

    Bea Lydeckers Naturals Inc is recalling Living Free Lung & Joint Congestion Herbal Dietary Supplement because the label declares lecithin but does not identify it as soy lecithin, creating an undeclared soy allergen hazard.

    Product
    Living Free Lung & Joint Congestion Herbal Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Lung & Joint Congestion Herbal Dietary Supplement***Glandular…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V550000·2021-07-21

    2020-2021 Bentley Continental GT Front Seat May Trap Rear Passenger Legs

    Bentley is recalling certain 2020-2021 Continental GT vehicles because the front seat may trap a rear passenger's legs during automated movements. The front seat software will be updated free of charge.

    Product
    BENTLEY — BENTLEY CONTINENTAL GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0781-2021·2021-07-21

    Living Free Nerve & Muscle Plus Supplement Recalled for Undeclared Soy

    Bea Lydeckers Naturals Inc is recalling Living Free Nerve & Muscle Plus Cetyl-Myristoleate supplement because the label declares lecithin but does not declare that the lecithin is soy-derived, posing a risk to consumers with soy allergies.

    Product
    Living Free Nerve & Muscle Plus Cetyl-Myristoleate Herbal and Glandular Supplement, 180 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Nerve & Muscle Plus Cetyl-Myristoleate…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateCPSC·21169·2021-07-21

    Rite Aid Recalls Rechargeable Handheld Fans Due to Fire Hazard

    Rite Aid is recalling about 9,780 rechargeable handheld fans sold nationwide from April through June 2021 because the lithium ion battery can overheat while charging and pose a fire hazard. The company has received two reports of the fans overheating and emitting smoke, though no injuries have been reported.

    Product
    Rechargeable handheld fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0659-2021·2021-07-21

    Durisan Hand Sanitizing Wipes Recalled for CGMP Deviations

    Sanit Technologies, LLC is recalling Durisan Antimicrobial Solutions Hand Sanitizing Wipes (benzalkonium chloride, 0.13%) due to manufacturing deviations that could result in contaminated product.

    Product
    Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing Wipes, 0.13%, packaged in 80-count canister (UPC 8 52379 00632 5), b) 160-count canister (UPC 8 52379 00631 8), and c) 240-count canister (UPC 8 52379 00633 2); Sanit Technologies, LLC, 7810 25th Court East…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2069-2021·2021-07-21

    Arrow Temporary Pacing Catheter Kit Recalled for Marketing Without FDA 510K Clearance

    Arrow International is recalling its Temporary Pacing Catheter/Introducer Kit (5 units) because it was marketed without FDA 510K clearance. Affected lot numbers: 16F20C0035 and 16F20F0124.

    Product
    Arrow Temporary Pacing Catheter/Introducer Kit 6Fr. pacing catheter 7Fr. introducer Product Code: AI-06210-IK - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0658-2021·2021-07-21

    Durisan Antimicrobial Hand Sanitizer Recalled for Manufacturing Deviations

    Sanit Technologies, LLC is recalling multiple lots of Durisan Antimicrobial Solutions hand sanitizer due to manufacturing deviations. The affected products were manufactured under the same conditions as contaminated lots.

    Product
    Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizer, listed as 0.1% or 0.13%, Alcohol-Free, packaged in a) 18 mL Net Content 0.61 fl oz credit card size container, (UPC 8 52379 00614 1); b) 50 mL Net Content 1.69 oz bottle, (UPC 8 52379 00634 9 and 8 52379…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0660-2021·2021-07-21

    Cipla Solifenacin Succinate Tablets Recalled for CGMP Deviations

    Cipla USA is recalling 7,228 bottles of Solifenacin Succinate Tablets, 10 mg (Lot #GG90819, expiring 06/2021) distributed nationwide due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Solifenacin Succinate Tablets, 10 mg, 30-count bottles, Rx Only, Manufactured by: Cipla Ltd., Verna, Goa, India Manufactured for Cipla USA, Inc. 1560 Sawgrass Corporate Parkway, Suite 130, Sunrise, FL, 33323, NDC 69097-261-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2067-2021·2021-07-21

    Medical device recall: Lingen SAMPLE Virus Sampling Kit lacks FDA clearance

    Mercedes Medical voluntarily recalled Lingen SAMPLE Virus Sampling Kits due to lack of FDA 510(k) clearance. The recall affects units distributed nationwide and internationally.

    Product
    Lingen SAMPLE Disposable Virus Sampling Kit pack, Item SAM ENI MTM-04, containing 2 tubes and 2 swabs/pack; and SAM ENI MTM04TUBE, containing 1 tube/pack.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2066-2021·2021-07-21

    Medical Device Recall: Lingen Disposable Virus Sampling Kit, No 510(k) Clearance

    The Lingen Disposable Virus Sampling Kit by Mercedes Medical was voluntarily recalled due to lacking FDA 510(k) clearance. The recall affected approximately 11,711 boxes distributed nationwide and internationally.

    Product
    Lingen Disposable Virus Sampling Kit, Item MTM-04, 40 tubes/box.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V543000·2021-07-20

    Newell P50 Recalled for Window Adhesive Failure Risk

    Newell Coach Corp. is recalling 2008-2022 P50 vehicles because window vent adhesive may fail, causing the vent to detach and increasing crash risk.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V546000·2021-07-20

    2022 Kenworth Medium-Duty Trucks Windshield Defrost Failure Recall

    Certain 2022 Kenworth T680, T880, and W990 trucks have defective HVAC controls that may fail to operate the windshield defrost system, reducing driver visibility and increasing crash risk. PACCAR is replacing the HVAC control heads free of charge.

    Product
    KENWORTH — KENWORTH T880, W900, T680
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V542000·2021-07-20

    2021 Newmar Ventana motorhomes recalled for loose tie rod clamps

    Newmar Corporation is recalling certain 2021 Ventana motorhomes because tie rod clamps may be loose, potentially causing tie rod ends to break or detach and resulting in steering loss.

    Product
    NEWMAR — NEWMAR KOUNTRY STAR, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V547000·2021-07-20

    School Bus Parking Brake May Fail, Increasing Crash Risk

    Daimler Trucks is recalling 267 school buses because the parking brake activation switch may fail to set the parking brake, increasing the risk of unintended vehicle movement and crashes.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V544000·2021-07-20

    Osage Super Warrior Recall for Display Lockup Hazard

    Osage Industries is recalling one 2021 Super Warrior vehicle because the emergency lighting display may lock up, potentially delaying emergency efforts.

    Product
    OSAGE — OSAGE SUPER WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V545000·2021-07-20

    2022 Tiffin Phaeton motorhomes recalled for fuel hose fire risk

    Tiffin is recalling 2021-2022 Phaeton and Allegro Bus motorhomes with certain Cummins L9 diesel engines for a potential fuel leak that could cause a fire. The leak occurs between the fuel pump and remote filter head.

    Product
    TIFFIN — TIFFIN PHAETON, ALLEGRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V540000·2021-07-20

    ShowHauler Recalls 2018-2020 Motorhomes Due to Window Adhesive Failure

    ShowHauler is recalling 2018-2020 Garage Coach, Toter Coach, and Motorhome vehicles because window vent adhesive may fail, posing a crash risk.

    Product
    SHOWHAULER — SHOWHAULER MOTORHOME, TOTER COACH, GARAGE COACH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·024-2021·2021-07-16

    Green Dining Table Inc. Recalls Frozen Pork Dumplings Due to Misbranding and Undeclared Allergens

    Green Dining Table Inc. is recalling frozen pork dumplings because milk and coconut allergens were not declared on labels, posing potential allergen risks to consumers.

    Product
    Green Dining Table, Inc. — Green Dining Table, Inc. Recalls Frozen Pork Dumplings Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V539000·2021-07-16

    Mercedes-Benz Recalls 2013 GLK250 Diesel Vehicles for Transmission Defect

    Mercedes-Benz is recalling 2013 GLK250 diesel vehicles because incorrect transmission parts may cause fluid leaks or module failure, increasing fire and crash risks.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLK250
    Category
    Vehicle
    Distribution
    Distributed nationwide