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.

Which agencies issued them

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.

1476–1500 of 80071

  • HighFDA (Devices)·Z-2293-2026·2026-06-10

    Arvis Hip and Knee 2.0 trackers may show wear and corrosion

    Arvis Hip & Knee 2.0 Instrument Sets are being recalled because the Impactor V-Block Assembly and Trackers may show early wear or corrosion on the exposed magnet face.

    Product
    Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2302-2026·2026-06-10

    BD Pyxis MedStation fingerprint scanners may overheat and cause burns

    BD Pyxis MedStation ES Tower medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.

    Product
    BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0569-2026·2026-06-10

    Family Wellness ultra strength antacid tablets contain metallic particles

    A further lot of Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, is being recalled because of small metallic particles in the chewable tablets.

    Product
    FAMILY WELLNESS, ULTRA STRENGT, ANTACID TABLETS, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: MIDWOOD BRANDS, LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA., UP: 0 32251-92282-4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0978-2026·2026-06-10

    Albertsons sub sandwich tray does not declare pistachio allergen

    Albertsons store-made Kitchen Tray Sub Sandwich is being recalled because the contains statement does not declare pistachio. 13 units are affected.

    Product
    UPC 29259700000 KITCHEN TRAY SUB SANDWICH 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
  • HighFDA (Devices)·Z-2297-2026·2026-06-10

    BD Pyxis MedStation 4000 fingerprint scanner may overheat and burn

    The BD Pyxis MedStation 4000 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 4000 REF: 303 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0578-2026·2026-06-10

    TopCare extra strength antacid tablets contain small metallic particles

    TopCare Health Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    TOPCARE EXTRA STRENGTH ANTACID — TOPCARE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0554-2026·2026-06-10

    Spectra lidocaine ampules recalled over lack of sterility assurance

    Lidocaine HCl Injection USP in 5 mL single-dose ampules distributed by Spectra Medical Devices is being recalled for lack of assurance of sterility. 210,625 ampules affected.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE ANHYDROUS)
    Category
    Drug
    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 (Devices)·Z-2281-2026·2026-06-10

    Covidien EndoStitch loading unit pouches may have sterility-breaking holes

    Covidien EndoStitch Polysorb Single Use Loading Units are being recalled because holes in the pouch may compromise the sterile barrier. 2,448 units are affected.

    Product
    Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0982-2026·2026-06-10

    Pavilions single serve banana nut muffins do not declare walnut

    Pavilions Banana Nut Muffins single serve, an Albertsons store-made item, are being recalled because the contains statement does not declare walnut. 55 units are affected.

    Product
    UPC 28994500000 PAVILIONS MUFFINS BANANA NUT SINGLE SERVE 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-2301-2026·2026-06-10

    BD Pyxis Mini Main cabinets may overheat at fingerprint scanner

    BD Pyxis Mini Main medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 709 units affected.

    Product
    BD Pyxis Mini Main REF: 349 Medication cabinet
    Category
    Medical Device
    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 (Drugs)·D-0574-2026·2026-06-10

    GoodSense antacid chewable tablets contain small metallic particles

    GoodSense Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of a foreign substance: small metallic particles in the chewable tablets.

    Product
    GOODSENSE EXTRA STRENGTH ANTACID — GOODSENSE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1030-2026·2026-06-10

    Chewie Susans thumbprint cookie snack platters do not declare pecan

    Albertsons store-made Platter Snack Chewie Susans Thumbprints is being recalled because the contains statement does not declare pecan. 158 units are affected.

    Product
    UPC 22304700000 PLATTER SNACK CHEWIE SUSANS THUMBPRINTS 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-1012-2026·2026-06-10

    Albertsons duo seafood salad with crackers does not declare whiting

    Albertsons store-made Ready Meals Duo Seafood Salad with Crackers is being recalled because the contains statement does not declare whiting. 286 units are affected.

    Product
    UPC 27183100000 Ready Meals DUO SEAFOOD SALAD W/CRACKERS 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-2296-2026·2026-06-10

    Avanta administration tube sets may not engage the flow control valve

    Avanta Multi-Patient Administration Tube Sets are being recalled because supplier changes created a fit issue, so the stopcock cannot be reliably engaged with the Contrast Flow Control Valve.

    Product
    Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1072-2026·2026-06-10

    Albertsons sweet chili salmon salad omits salmon and walnut declarations

    Albertsons store-made Fresh Berry & Sweet Chili Salmon Salad is being recalled because the contains statement does not declare salmon and walnut. Four units are affected.

    Product
    UPC 21478000000 Ready Meals SALAD FRESH BERRY & SWEET CHILI Salmon 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
  • HighFDA (Food)·H-1038-2026·2026-06-10

    Albertsons kale berry feta salad does not declare walnut

    Albertsons store-made Kale Berry Feta Salad is being recalled because the contains statement does not declare walnut. 31 units are affected.

    Product
    UPC 29472300000 SALAD KALE BERRY FETA FS COLD UPC 29472100000 Ready Meals SALAD KALE BERRY FETA 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 (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 (Food)·H-1026-2026·2026-06-10

    Albertsons Cheeses of France platter does not declare almond

    Albertsons store-made Platter Cheeses of France is being recalled because the contains statement does not declare almond. 31 units are affected.

    Product
    UPC 27837800000 PLATTER CHEESES OF FRANCE 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-0905-2026·2026-06-10

    Second Nature Keto Crunch mix may contain undeclared cashews and pistachios

    Second Nature Keto Crunch Smart Mix is being recalled because the product may contain undeclared allergens, specifically cashews and pistachios, along with dried cherries.

    Product
    SECOND NATURE KETO CRUNCH SMART MIX, 10-ounce retail-sized plastic pouch, UPC 077034013405, 6-10oz units per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2291-2026·2026-06-10

    Philips Azurion 7M20 Roadmap Pro may produce unusable dark images

    Philips Azurion 7M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 7M20, Model Numbers: 722079, 722224 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
  • HighFDA (Drugs)·D-0564-2026·2026-06-10

    Market Basket ultra strength antacid tablets contain small metallic particles

    Market Basket Antacid, calcium carbonate 1000 mg ultra strength, is being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    MARKET BASKET ANTACID Calcium Carbonate 1000 mg, ULTRA STRENGTH, 72 Tablets, Distributed by: De Moules Supermarkets, Inc.,Tewksbury, Mass 01875, UPC 0 49705 83149 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0988-2026·2026-06-10

    Albertsons 16-inch carving tray does not declare walnut

    An Albertsons store-made 16-inch carving tray is being recalled because the contains statement does not declare walnut. 12 units are affected.

    Product
    UPC 29168800000 CARVING TRAY 16IN FS 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