The Recall Desk

State

Kentucky product recalls

72,907 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.

These figures cover only the 7,164 recalls whose distribution notice names Kentucky specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1451–1475 of 80071

  • SevereFDA (Food)·H-0907-2026·2026-06-10

    Cheese sauce mixes contain dry milk powder recalled over Salmonella

    Cheese Sauce Mix and Creamier Cheese Sauce Mix are being recalled because they contain a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0399549125016 2) Cheese Sauce Mix, 25 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954924308 3) Creamier Cheese Sauce Mix, 25 lb., packaged in a tied poly bag an
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Devices)·Z-2278-2026·2026-06-10

    Design Options spinal trays recalled over Huons bupivacaine quality issues

    Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.

    Product
    Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINAL CUST) (560272), SSK CA P M C (ORIGINAL CUST) (560327), SSK T M H (560394), SSK S O 20070208 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2253-2026·2026-06-10

    BD combined Whitacre and Quincke spinal trays recalled over bupivacaine

    BD Spinal Trays containing both a Whitacre 25 G and a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 290 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2223-2026·2026-06-10

    Ivenix pump software may report false battery health and shut down

    The Ivenix Infusion System Large Volume Pump software is being recalled because a software anomaly can report a false battery-health value and trigger a shutdown alarm.

    Product
    LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2254-2026·2026-06-10

    BD Whitacre 25 gauge spinal trays recalled over bupivacaine quality issues

    BD Spinal Trays with a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0910-2026·2026-06-10

    Cold prep cream sauce contains dry milk recalled for Salmonella

    Cold Prep Cream Sauce in 20 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Devices)·Z-2248-2026·2026-06-10

    BD Quincke spinal trays recalled over Huons bupivacaine quality issues

    BD Spinal Trays with a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 990 units are affected.

    Product
    BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2252-2026·2026-06-10

    BD Whitacre 24 gauge spinal trays recalled over bupivacaine quality issues

    BD Spinal Trays with a Whitacre 24 G needle, catalog numbers 400868 and 405652, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,550 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2295-2026·2026-06-10

    Phothera 200 phototherapy calibration certificates had outputs reversed

    Phothera 200 phototherapy devices are being recalled because some Calibration and Output Certificates had the outputs reversed. 368 units are affected.

    Product
    Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2298-2026·2026-06-10

    BD Pyxis MedStation ES fingerprint scanner may overheat and burn

    The BD Pyxis MedStation ES medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.

    Product
    BD Pyxis MedStation ES REF: 323 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1023-2026·2026-06-10

    Pad Thai chicken ready meals do not declare anchovy

    Albertsons store-made Wok Pad Thai Chicken ready meals are being recalled because the contains statement does not declare anchovy.

    Product
    UPC 21208300000 Ready Meals WOK PAD THAI CHICKEN SS COLD 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
  • HighFDA (Food)·H-1018-2026·2026-06-10

    Albertsons caesar salads do not declare anchovy allergen

    Albertsons store-made Kitchen Caesar Salads in large and small sizes are being recalled because the contains statement does not declare anchovy. 39 units are affected.

    Product
    UPC 29787600000 Kitchen SALAD CAESAR LARGE SS COLD UPC 21543200000 Kitchen SALAD CAESAR SMALL 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
  • HighFDA (Devices)·Z-2304-2026·2026-06-10

    BD Pyxis MedBank Mini fingerprint scanner may overheat and burn

    The BD Pyxis MedBank Mini medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.

    Product
    BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1047-2026·2026-06-10

    Albertsons ahi poke products do not declare tuna allergen

    Albertsons store-made ahi poke products, sold under three UPCs, are being recalled because the contains statement does not declare tuna. 23 units in total are affected.

    Product
    UPC 23952700000 POKE AHI LIMU UPC 23506700000 POKE AHI LIMU PREVIOUSLY FROZEN - CO UPC 23958200000 POKE AHI SALT & PEPPER This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scal
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0577-2026·2026-06-10

    Equaline ultra strength antacid tablets contain small metallic particles

    Equaline Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    EQU ULTRA STRENGTH ANTACID ASSORTED FRUIT 171AF — EQU ULTRA STRENGTH ANTACID ASSORTED FRUIT 171AF (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2308-2026·2026-06-10

    Stapes prosthesis pistons carry an incorrect functional length on labeling

    Titanium/fluoroplastic piston stapes prostheses are being recalled because the device labeling states an incorrect functional length. Seven units are affected.

    Product
    TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2279-2026·2026-06-10

    CASE cardiac testing systems may spark at the printer head

    CASE v7.0 Cardiac Testing Systems are being recalled because electrical sparking may occur at the printer head, and ignition of thermal paper could cause serious thermal injury.

    Product
    CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2275-2026·2026-06-10

    PhaseOne antimicrobial solution sprayer springs may corrode into the product

    PhaseOne Antimicrobial Solution is being recalled because the stainless steel spring inside the sprayer can corrode, releasing trace metallic elements into the solution.

    Product
    PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0962-2026·2026-06-10

    Chocolate lady madeleine strawberry cakes do not declare almond allergen

    Albertsons store-made Cake Pav Chocolate Lady Madeleines Strawberry is being recalled because the contains statement does not declare almond. Six units are affected.

    Product
    UPC 25491700000 Cake Pav Chocolate Lady Madeleines Strawberry. 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
  • HighFDA (Food)·H-0980-2026·2026-06-10

    Albertsons banana nut muffins do not declare walnut allergen

    Albertsons store-made Banana Nut Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 434 units are affected.

    Product
    UPC 22454900000 MUFFINS BANANA NUT 2CT UPC 22120200000 MUFFINS BANANA NUT 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
  • HighFDA (Food)·H-0958-2026·2026-06-10

    Albertsons colossal Dubai cheesecake slice does not declare pistachio

    Albertsons store-made Cheesecake Slice Colossal Dubai is being recalled because the contains statement does not declare pistachio. 32 units are affected.

    Product
    UPC 25216200000 Cheesecake Slice Colossal Dubai. 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
  • HighFDA (Food)·H-0963-2026·2026-06-10

    Albertsons raspberry moon cake does not declare almond allergen

    Albertsons store-made Cake Raspberry Moon 8-inch 2-layer is being recalled because the contains statement does not declare almond. 25 units are affected.

    Product
    UPC 25811100000 CAKE RASPBERRY MOON 8IN 2-layer. 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
  • HighFDA (Drugs)·D-0572-2026·2026-06-10

    Hy-Vee ultra strength antacid tablets contain small metallic particles

    Hy-Vee Ultra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    HyVee, Ultra Strength Antacid, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: HY-VEE INC., Inc., WEST DES MOINES, IA 50266, UPC: 0 75450 82514 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1021-2026·2026-06-10

    Albertsons grilled chicken salad does not declare almond allergen

    Albertsons store-made Kitchen Salad Grilled Chicken is being recalled because the contains statement does not declare almond. 27 units are affected.

    Product
    UPC 27163100000 Kitchen SALAD GRILLED CHICKEN 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
  • HighFDA (Food)·H-1025-2026·2026-06-10

    Pad Thai chicken with pot stickers does not declare anchovy

    Albertsons store-made Ready Meals Wok Pad Thai Chicken with Pot Stickers is being recalled because the contains statement does not declare anchovy. 39 units are affected.

    Product
    UPC 21380100000 Ready Meals WOK PAD THAI CHICKEN WITH POT STICKERS SS 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