The Recall Desk

State

Kentucky product recalls

72,913 recalls have nationwide distribution and so reach Kentucky. 7,164 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total
7,164
Critical
1,399
Severe
1,694
Most recent
2026-09-09

Of the 7,164 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.

Which agencies issued them

These figures cover only the 7,164 recalls whose distribution notice names Kentucky specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1651–1675 of 80077

  • ModerateFDA (Food)·H-1063-2026·2026-06-10

    Albertsons piri piri marinated Atlantic salmon portions omit salmon declaration

    Albertsons store-made Salmon Atlantic Portion Piri Piri Marinade is being recalled because the contains statement does not declare salmon. 108 units are affected.

    Product
    UPC 23100200000 SALMON ATLANTIC PORTION PIRI PIRI MARINADE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0598-2026·2026-06-10

    Xyvona levorphanol tablets recalled after FDA denied the proprietary name

    Xyvona levorphanol tartrate tablets, 2 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.

    Product
    Xyvona (levorphanol tartrate tablets), 2mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NV 89113, NDC 72245-762-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0957-2026·2026-06-10

    Albertsons yellow fudge pecan cake omits pecan from contains statement

    Albertsons store-made Cake Yellow Fudge Pecan half 8-inch is being recalled because the contains statement does not declare pecan.

    Product
    UPC 28848900000 Cake Yellow Fudge Pecan 1/2 8IN This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1009-2026·2026-06-10

    Albertsons Old Bay seasoned shrimp omits shrimp declaration

    Albertsons store-made Shrimp P&D Old Bay Seasoned is being recalled because the contains statement does not declare shrimp. Five units are affected.

    Product
    UPC 23036500000 SHRIMP P&D OLD BAY SEASONED This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1049-2026·2026-06-10

    Albertsons tuna pickle snacker salad omits tuna declaration

    Albertsons store-made Snacker Salad Tuna Pickle is being recalled because the contains statement does not declare tuna. Seven units are affected.

    Product
    UPC 29132100000 KITCHEN SNACKER SALAD TUNA PICKLE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0552-2026·2026-06-10

    Eugia lidocaine vial label wrap covers the barcode

    Eugia Lidocaine HCl Injection, USP 2% single-dose vials are being recalled because the label wrap covers the barcode, making it hard to scan. 168,300 vials are affected.

    Product
    LIDOLOG KIT — LIDOLOG KIT (LIDOCAINE, KENALOG, POVIDONE IODINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2285-2026·2026-06-10

    Philips Azurion 3M15 Medical Imaging Systems Recalled Due to Software Issue

    Philips Medical Systems is recalling 27 Philips Azurion 3M15 units because a software issue can cause unusable dark images during imaging procedures.

    Product
    Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1068-2026·2026-06-10

    Albertsons citrus lemon salmon kabobs omit salmon declaration

    Albertsons store-made Salmon Kabob with Citrus Lemon Marinade is being recalled because the contains statement does not declare salmon.

    Product
    UPC 23180600000 SALMON KABOB With CITRUS LEMON MARINADE This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0973-2026·2026-06-10

    Albertsons almond raspberry croissants omit almond from contains statement

    Albertsons store-made Almond Raspberry Filled Croissants, 4 count, are being recalled because the contains statement does not declare almond. 15 units are affected.

    Product
    UPC 25317100000 CROISSANTS ALMOND RASPBERRY FILLED 4CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0976-2026·2026-06-10

    Albertsons tuna salad croissant sandwich omits tuna from contains statement

    Albertsons store-made Ready Meals Sandwich Tuna Salad Croissant is being recalled because the contains statement does not declare tuna. 156 units are affected.

    Product
    UPC 21788400000 Ready Meals SANDWICH TUNA SALAD CROISSANT SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0599-2026·2026-06-10

    Xyvona 3 mg levorphanol tablets recalled after proprietary name denial

    Xyvona levorphanol tartrate tablets, 3 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.

    Product
    Xyvona (levorphanol tartrate tablets), 3mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NV 89113, NDC 72245-058-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2265-2026·2026-06-10

    B. Braun spinal epidural catheters contain Mastisol with cracking tubing

    B. Braun NES1725KFXL spinal epidural closed tip catheters are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack. 1,730 units affected.

    Product
    Brand Name: B. BRAUN MEDICAL INC. Product Name: NES1725KFXL SPINAL EPID CLOSED TIP CATH Model/Catalog Number: 530201 Software Version: N/A Product Description: NES1725KFXL SPINAL EPID CLOSED TIP CATH Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1053-2026·2026-06-10

    Albertsons wild salmon feta spinach burger omits salmon declaration

    Albertsons store-made Wild Salmon Feta Spinach Burger is being recalled because the contains statement does not declare salmon. One unit is affected.

    Product
    UPC 23258300000 BURGER WILD SALMON FETA SPINACH This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1050-2026·2026-06-10

    Albertsons quad tuna salad omits tuna from contains statement

    Albertsons store-made Quad Tuna Salad is being recalled because the contains statement does not declare tuna. 133 units are affected.

    Product
    UPC 21500300000 READY MEALS QUAD TUNA SALAD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V371000·2026-06-09

    Ford Recalls 2024 Explorers for Potential Park System Damage

    Ford is recalling 2024 Explorer vehicles with 2.3L engines and 10R60 transmissions because an unintentional powertrain control module reset may damage the park system, increasing the risk of vehicle rollaway.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E033000·2026-06-09

    Cummins CNG Fuel System Recall for Tank Bracket Deformation Risk

    Natural Gas Fuel Systems is recalling Cummins CNG fuel systems because the tank support bracket may deform in a side impact, potentially causing the tank to detach and leak fuel.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY:MOUNTING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V376000·2026-06-09

    Ford Recalls Focus and Fusion Vehicles for Transmission Clutch Fracture Risk

    Ford is recalling 2015-2018 Focus and 2013-2016 Fusion vehicles previously repaired incorrectly under prior recalls. The clutch may fracture, causing transmission damage and fluid leaks that increase fire risk.

    Product
    FORD — FORD FOCUS, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V378000·2026-06-09

    Ford Recalls 2014 F-150s for Transmission Software Update

    Ford is recalling 2014 F-150 vehicles previously repaired under recall 24V444 because a signal loss can cause unexpected downshifting, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V369000·2026-06-09

    Ford Recalls 2012-2018 Focus Vehicles for Engine Stall Risk

    Ford is recalling 2012-2018 Focus vehicles previously repaired under recall 18V735 because a malfunctioning Canister Purge Valve may cause the engine to stall while driving, increasing crash risk.

    Product
    FORD — FORD FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V368000·2026-06-09

    Ford Recalls 2018-2024 Expeditions for Center Console Sharp Edges

    Ford is recalling 2018-2024 Expedition vehicles because chrome plating on the center console may peel, creating sharp edges that could injure occupants.

    Product
    FORD — FORD EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V375000·2026-06-09

    Ford Recalls 2018 F-150s for Transmission Software Defect

    Ford is recalling 2018 F-150 vehicles previously repaired under recall 17V669 due to a software defect that may cause unintended gear selection and loss of gear indication.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V377000·2026-06-09

    Ford Recalls 2019 Lincoln Nautilus for Lane Center Assist Software Defect

    Ford is recalling 2019 Lincoln Nautilus vehicles previously repaired under recall 19V031 because the lane center assist system may fail to detect if the driver's hands are off the steering wheel for a prolonged period.

    Product
    LINCOLN — LINCOLN NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V373000·2026-06-09

    Ford Recalls 2018-2020 F-150s for Daytime Running Lamp Defect

    Ford is recalling 2018-2020 F-150 vehicles previously repaired under recall 20V097 because daytime running lamps may fail to dim, reducing visibility for other drivers.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide