The Recall Desk

State

Idaho product recalls

72,907 recalls have nationwide distribution and so reach Idaho. 3,517 additional recalls listed Idaho specifically in their distribution scope.

What the numbers show

Total
3,517
Critical
364
Severe
1,023
Most recent
2026-09-06

Of the 3,517 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,023 (29%) are Severe.

These figures cover only the 3,517 recalls whose distribution notice names Idaho 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 76424

  • HighFDA (Food)·H-1031-2026·2026-06-10

    Albertsons lox avocado toast does not declare salmon allergen

    Albertsons store-made Lox Avocado Toast is being recalled because the contains statement does not declare salmon. 19 units are affected.

    Product
    UPC 21299900000 LOX AVOCADO TOAST FS 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-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-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 (Devices)·Z-2289-2026·2026-06-10

    Philips Azurion 7B20/15 systems may show unusable dark fluoroscopy images

    Philips Azurion 7B20/15 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable. 156 units affected.

    Product
    Philips Azurion 7B20/15, Model Numbers: 722068, 722226 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 (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 (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-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
  • HighFDA (Drugs)·D-0573-2026·2026-06-10

    H-E-B extra strength antacid tablets contain small metallic particles

    H.E.B Extra Strength Calcium Carbonate Antacid Tablets, 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    HEB EXTRA STREGTH ANTACID — HEB EXTRA STREGTH ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    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 (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-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 (Food)·H-0981-2026·2026-06-10

    Cream cheese filled banana nut muffins do not declare walnut

    Albertsons store-made Muffins Banana Nut Cream Cheese Filled 2 count are being recalled because the contains statement does not declare walnut. Nine units are affected.

    Product
    UPC 25312600000 MUFFINS BANANA NUT CREAM CHEESE FILLED 2CT 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-0991-2026·2026-06-10

    Albertsons 16-inch Italian sampler tray does not declare almond

    An Albertsons store-made 16-inch Italian sampler tray is being recalled because the contains statement does not declare almond. Nine units are affected.

    Product
    UPC 29153000000 SAMPLER TRAY ITALIAN 16 INCH 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-2292-2026·2026-06-10

    Arvis Hip and Knee 3.0 trackers may show wear and corrosion

    Arvis Hip & Knee 3.0 Instrument Sets are being recalled because the V-Block Assembly and Trackers A, B, C and E may show early wear or corrosion on the exposed magnet face.

    Product
    Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1002-2026·2026-06-10

    Albertsons cilantro lime shrimp does not declare anchovy allergen

    Albertsons store-made Shrimp 41-50 P&D with Cilantro Lime Marinade is being recalled because the contains statement does not declare shrimp and anchovy.

    Product
    UPC 23168600000 SHRIMP 41-50 P&D With CILANTRO LIME MARINADE 5% 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-0959-2026·2026-06-10

    Albertsons catering loaf cake platter does not declare walnut

    Albertsons store-made Platter Catering Loaf Cake Slice is being recalled because the contains statement does not declare walnut. 92 units are affected.

    Product
    UPC 22418000000 Platter Catering Loaf Cake Slice. 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-1034-2026·2026-06-10

    Albertsons peanut butter chocolate chip bars do not declare almond

    Albertsons store-made Peanut Butter Chocolate Chip Bar with Pretzel is being recalled because the contains statement does not declare almond. 128 units are affected.

    Product
    UPC 24144500000 Ready Meals PEANUT BUTTER CHOCOLATE CHIP BAR With PRETZEL 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-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 (Drugs)·D-0563-2026·2026-06-10

    7-Eleven antacid chewable tablets contain small metallic particles

    24/7 life by 7-Eleven Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    24/7 life BY 7-ELEVEN, Extra strength Antacid Tablets, Calcium Carbonate 750 mg, 96 chewable tablets, DISTRIBUTED BY 7-ELEVEN, IRVING, TX 75063, UPC 0 5254863573 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0960-2026·2026-06-10

    Albertsons white strawberry cake bars do not declare almond

    Albertsons store-made Artisan White Strawberry Cake Bar is being recalled because the contains statement does not declare almond. 173 units are affected.

    Product
    UPC 22253500000 Cake Bar Artisan White Strawberry Small. 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-2306-2026·2026-06-10

    GE MAC 5 ECG systems may link data to the wrong patient

    GE MAC 5 A4 and A5 Resting ECG Analysis Systems are being recalled because a development software version was released that can associate clinical information with the wrong patient.

    Product
    MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph
    Category
    Medical Device
    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
  • 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