The Recall Desk

State

Kentucky product recalls

73,495 recalls have nationwide distribution and so reach Kentucky. 7,202 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total
7,202
Critical
1,409
Severe
2,024
Most recent
2026-10-14

Of the 7,202 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.

These figures cover only the 7,202 recalls whose distribution notice names Kentucky specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23051–23075 of 80697

  • SevereFDA (Drugs)·D-0725-2022·2022-03-23

    Avaphinal Maximum Male Enhancement Pills Recalled for Undeclared Drug

    Walmart is recalling Avaphinal Maximum Male Enhancement Sexual Pills (2000 MG, 10-capsule cartons, Lot DK1027) distributed nationwide because they contain undeclared sildenafil, making them an unapproved drug.

    Product
    Avaphinal Maximum Male Enhancement Sexual Pills, 2000 MG*, packaged in 10 Capsules per carton.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0862-2022·2022-03-23

    Helmi Honey VIP Recalled for Undisclosed Drug Ingredient

    Helmi Honey VIP is being recalled nationwide due to the presence of an undisclosed drug ingredient. Consumers should stop using the product and return it.

    Product
    Helmi Honey VIP packaged in a gold paper box with black writing, 12 sachets per box UPC 3553314122014
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0780-2022·2022-03-23

    RX CHOLANGIOGRAM KIT recalled due to sterile barrier breach

    Boston Scientific is recalling RX CHOLANGIOGRAM KIT due to a sterile barrier breach that compromises device sterility. Approximately 500 units distributed worldwide are affected.

    Product
    RX CHOLANGIOGRAM KIT Material Numbers: M00575241 M00575281 M00575321 M00575361 M00575381 M00575401 M00575441 M00575481
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0883-2022·2022-03-23

    Stutzman Farms Sourdough Einkorn Pretzels Recalled for Undeclared Wheat

    Stutzman Farms is recalling 4oz and 8oz bags of Sourdough Einkorn Pretzels due to undeclared wheat allergen. Consumers with wheat allergies should not consume this product.

    Product
    Stutzman Farms Sourdough Einkorn Pretzels sold in 4oz and 8oz bags
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0752-2022·2022-03-23

    Boston Scientific Sphincterotome Recalled for Sterile Barrier Breach

    Boston Scientific Corporation is recalling 1,811 units of Dreamtome Cannulating Sphincterotomes worldwide because the sterile barrier is compromised, creating a potential contamination risk.

    Product
    Dreamtome Cannulating Sphincterotome-DREAMTOME 44-20MM/450CM Material Number: M00584060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0754-2022·2022-03-23

    Boston Scientific DREAMTOME Medical Device Recalled for Sterile Barrier Breach

    Boston Scientific is recalling 142 units of DREAMTOME 44-30MM/450CM medical devices distributed worldwide due to a sterile barrier breach that compromises device sterility. Affected lot numbers are 27625066 and 27805561.

    Product
    DREAMTOME 44-30MM/450CM Material Number: M00584070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0783-2022·2022-03-23

    Traverse Rail Carrier E-System components with defective short screws

    Hill-Rom Traverse Rail Carrier E-System components contain non-conforming screws that are too short to secure the rail properly. The screws could loosen over time, causing the rail system to fall and potentially injure caregivers or patients.

    Product
    (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX component to Liko overhead lift. Intended for to make safe lifting of a patient possible. Affected Devices: 3101704 TRAV RAIL CARR E-SYST STD 3102514 TR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0808-2022·2022-03-23

    GE CARESCAPE Central Station audio alarms may be muted with unapproved keyboard

    GE Healthcare is recalling 10,445 CARESCAPE Central Station monitoring systems. If connected to an unapproved keyboard, audio alarms may be muted, potentially preventing users from receiving critical notifications.

    Product
    GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated), REF 2082278-001, and MAS700 (Desktop, REF 2082279-001.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0779-2022·2022-03-23

    Boston Scientific JAGTOME RX Device Recalled for Sterile Barrier Breach

    Boston Scientific is recalling 14 JAGTOME RX medical devices worldwide due to a sterile barrier breach that compromises the device's sterility.

    Product
    JAGTOME RX 49-30-450-035 Material Number: M00573030
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0793-2022·2022-03-23

    Adult Lumbar Puncture Drug Free Tray Recalled for Manometer Leaking

    Bard Peripheral Vascular Inc is recalling 1,260 Adult Lumbar Puncture Drug Free Trays due to manometer leaking and mating issues that could affect device function.

    Product
    ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0777-2022·2022-03-23

    Boston Scientific JAGTOME RX Medical Device Recalled for Sterile Barrier Breach

    Boston Scientific is recalling 101 units of JAGTOME RX devices due to compromised sterile barriers that could allow contamination and infection. The recall affects devices distributed worldwide.

    Product
    JAGTOME RX 49-20-260-035 Material Number: M00573000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0882-2022·2022-03-23

    Stutzman Farms Organic Einkorn Berries Recalled for Undeclared Wheat Allergen

    Stutzman Farms is recalling its organic einkorn berries due to undeclared wheat allergen. The recalled products were sold in bulk or in 25lb and 50lb bags across multiple states.

    Product
    Stutzman Farms Organic Einkorn Berries sold in bulk, or in 25lb and 50lb bags
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0772-2022·2022-03-23

    Medical device sterile barrier breach compromises sterility in JAGTOME RX

    Boston Scientific is recalling 98 JAGTOME RX medical devices due to a sterile barrier breach. The affected units were distributed worldwide.

    Product
    JAGTOME RX 39-30-450-025 Material Number: M00573110
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0895-2022·2022-03-23

    Fresh Creative Foods Chicken Enchilada Kit Recalled for Plastic Contamination

    Fresh Creative Foods is recalling its Red Sauce Chicken Enchilada Kit due to plastic pieces discovered during manufacturing. The contamination came from ice supplied to the manufacturer.

    Product
    Fresh Creative Foods RED SAUCE CHICKEN ENCHILADA KIT ON PREMISE NO TRAYS 2/6.75 LB UPC: 10013454381929 Item # 404979 Perishable/Keep refrigerated Kit components: 2/32 oz. bags of seasoned chicken w/rib meat, 8/8 pz. bags of Cryo Traditional Red Enchilada Sauce, 8 bags of…
    Category
    Food
    Distribution
    20 states
  • HighFDA (Food)·F-0880-2022·2022-03-23

    Stutzman Farms Sprouted Einkorn Crackers recalled for undeclared wheat allergen

    Stutzman Farms is recalling Sprouted Einkorn Crackers sold in 0.30lb and 1lb bags due to undeclared wheat allergen. The affected product was distributed in Indiana, Kentucky, Michigan, Missouri, Ohio, Pennsylvania, and Wisconsin.

    Product
    Stutzman Farms Sprouted Einkorn Crackers sold in .30lb and 1lb bags
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0757-2022·2022-03-23

    Boston Scientific DREAMTOME Stent Devices Recalled for Sterility Compromise

    Boston Scientific is recalling 472 DREAMTOME stent devices due to sterile barrier breach affecting product sterility. Devices were distributed worldwide including the US.

    Product
    DREAMTOME 49-30MM/260CM Material Number: M00584010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0760-2022·2022-03-23

    Hydratome RX 44-20MM medical device recalled for sterile barrier breach

    Boston Scientific is recalling 254 units of the Hydratome RX 44-20MM medical device worldwide due to a compromised sterile barrier that may affect device sterility.

    Product
    HYDRATOME RX 44-20MM/450CM Material Number: M00583060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0755-2022·2022-03-23

    Boston Scientific DREAMTOME medical devices recalled for sterile barrier breach

    Boston Scientific is recalling 982 units of DREAMTOME medical devices due to sterile barrier breach that compromises device sterility. Affected units were distributed worldwide.

    Product
    DREAMTOME 49-20MM/260CM Material Number: M00584000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0792-2022·2022-03-23

    FDA Recalls Adult Lumbar Puncture Trays for Manometer and Connector Defects

    Bard Peripheral Vascular is recalling 116,770 adult lumbar puncture trays due to manometer leaks and connector mating defects that could affect procedure performance.

    Product
    LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V177000·2022-03-23

    Bentley seat belt assembly defect may impair child restraint function

    Bentley Motors is recalling certain 2020-2022 Continental GT and Flying Spur vehicles due to incorrectly installed front seat belt assemblies that may lack an automatic locking retractor, potentially failing to secure child restraints properly in a crash.

    Product
    BENTLEY — BENTLEY CONTINENTAL GT, FLYING SPUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0890-2022·2022-03-23

    Thai Noodle Salad Recalled for Plastic Fragments

    Fresh Creative Foods is recalling Thai Noodle Salad due to hard clear plastic pieces found during manufacturing. The contamination originated from ice supplied to the manufacturer.

    Product
    Fresh Creative Foods THAI NOODLE SALAD NO CORN BULK 2/5 LB Kroger UPC: 10013454381974 Item # 404972 Distributed by Fresh Creative Foods, Vista, CA 92081
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-0751-2022·2022-03-23

    Boston Scientific Sphincterotome Device Recalled Due to Sterile Barrier Breach

    Boston Scientific is recalling 21,309 units of the Dreamtome RX Cannulating Sphincterotome due to a sterile barrier breach that compromises device sterility, creating a potential infection risk to patients.

    Product
    Dreamtome RX Cannulating Sphincterotome-DREAMTOME 44-20MM/260CM Material Number: M00584040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0774-2022·2022-03-23

    Medical Device JAGTOME RX Recalled for Compromised Sterile Barrier

    Boston Scientific is recalling 3,578 units of the JAGTOME RX medical device because the sterile barrier is compromised, which can allow contamination. The affected units were distributed worldwide.

    Product
    JAGTOME RX 44-20-450-035 Material Number: M00573050
    Category
    Medical Device
    Distribution
    Distributed nationwide