The Recall Desk

State

Kansas product recalls

72,907 recalls have nationwide distribution and so reach Kansas. 5,723 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,723
Critical
1,045
Severe
1,228
Most recent
2026-09-02

Of the 5,723 recalls naming Kansas we have scored against our rubric, 1,045 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,228 (21%) are Severe.

These figures cover only the 5,723 recalls whose distribution notice names Kansas specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1526–1550 of 78630

  • HighFDA (Drugs)·D-0566-2026·2026-06-10

    CareOne ultra strength antacid tablets contain small metallic particles

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

    Product
    ULTRA STRENGTH ANTACID ASSORTED BERRIES — ULTRA STRENGTH ANTACID ASSORTED BERRIES (CALCIUM CARBONATE)
    Category
    Drug
    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-2287-2026·2026-06-10

    Philips Azurion 5M20 Roadmap Pro may produce unusable dark images

    Philips Azurion 5M20 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 5M20, Model Numbers: 722228 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 (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
  • HighFDA (Devices)·Z-2299-2026·2026-06-10

    BD Pyxis Anesthesia Station fingerprint scanner may overheat and burn

    The BD Pyxis Anesthesia Station ES is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 4,579 units affected.

    Product
    BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0993-2026·2026-06-10

    Albertsons cocktail tray does not declare almond allergen

    An Albertsons store-made cocktail tray is being recalled because the contains statement does not declare almond.

    Product
    UPC 29133000000 TRAY COCKTAIL 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-2309-2026·2026-06-10

    Sharpoint microsurgical knives labeled 2.2mm actually measure 3.0mm

    Sharpoint 2.2 mm angled double-bevel microsurgical knives are being recalled because 3.0 mm knives were labeled and packaged as 2.2 mm. 1,818 units affected.

    Product
    Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife
    Category
    Medical Device
    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-0986-2026·2026-06-10

    Dubai chocolate parfait cups do not declare pistachio allergen

    Albertsons store-made Parfait Cup Dubai Chocolate is being recalled because the contains statement does not declare pistachio. 25 units are affected.

    Product
    UPC 25606600000 PARFAIT CUP DUBAI CHOCOLATE 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-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-1073-2026·2026-06-10

    Albertsons berry and salmon salad omits salmon and walnut declarations

    Albertsons store-made Fresh Berry & Salmon Salad is being recalled because the contains statement does not declare salmon and walnut. 90 units are affected.

    Product
    UPC 21477700000 Ready Meals SALAD FRESH BERRY & SALMON 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-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 (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 (Drugs)·D-0570-2026·2026-06-10

    Harris Teeter ultra strength antacid tablets contain metallic particles

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

    Product
    Harris Teeter, ULTRA STRENGTH ANTACID, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, Distributed by: Harris Teeter, LLC.,MATTHEWS, NC 28105, UPC: 0 72036-73108-1.
    Category
    Drug
    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 (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-1017-2026·2026-06-10

    Albertsons apple waldorf salad does not declare walnut allergen

    Albertsons store-made Apple Waldorf Salad is being recalled because the contains statement does not declare walnut. 33 units are affected.

    Product
    UPC 21633500000 READY MEALS SALAD APPLE WALDORF SS UPC 29824500000 Kitchen SALAD APPLE WALDORF FS UPC 27169500000 Kitchen SALAD APPLE WALDORF LRG UPC 27170300000 Kitchen SALAD APPLE WALDORF MED UPC 27169300000 Kitchen SALAD APPLE W
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0983-2026·2026-06-10

    Albertsons sticky bran muffins do not declare walnut allergen

    Albertsons store-made Sticky Bran Muffins, 4 count, are being recalled because the contains statement does not declare walnut. 105 units are affected.

    Product
    UPC 25524000000 MUFFINS STICKY BRAN 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 (Drugs)·D-0575-2026·2026-06-10

    GoodSense ultra strength antacid tablets contain small metallic particles

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

    Product
    GOODSENSE ULTRA STRENGTH ANTACID ASSORTED FRUIT — GOODSENSE ULTRA STRENGTH ANTACID ASSORTED FRUIT (CALCIUM CARBONATE)
    Category
    Drug
    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-0556-2026·2026-06-10

    Ascend amlodipine and olmesartan tablets failed dissolution specifications

    Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, are being recalled after failing dissolution specifications, with olmesartan medoxomil content below specification.

    Product
    AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0994-2026·2026-06-10

    Albertsons Twisted Bliss pretzel trays do not declare almond allergen

    Albertsons store-made Twisted Bliss Pretzel Tray is being recalled because the contains statement does not declare almond. Two units are affected.

    Product
    UPC 29344500000 TWISTED BLISS PRETZEL TRAY 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-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 (Food)·H-0969-2026·2026-06-10

    Albertsons cowboy cookies 18 count do not declare pecan allergen

    Albertsons store-made Cookies Cowboy 18 count is being recalled because the contains statement does not declare pecan. 982 units are affected.

    Product
    UPC 22730900000 COOKIES COWBOY 18CT 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-1029-2026·2026-06-10

    Albertsons sliced loaf platter does not declare walnut allergen

    Albertsons store-made Platter Loaf Sliced, 20 count, is being recalled because the contains statement does not declare walnut. 20 units are affected.

    Product
    UPC 22650200000 PLATTER LOAF SLC 20CT 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