The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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1501–1525 of 89454

  • 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-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 (Food)·H-1027-2026·2026-06-10

    Albertsons mini breakfast pastry platter does not declare almond

    Albertsons store-made Platter Pastry Mini Breakfast, 28 count, is being recalled because the contains statement does not declare almond. 75 units are affected.

    Product
    UPC 25081900000 PLATTER PASTRY MINI BREAKFAST 28CT 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 (Devices)·Z-2288-2026·2026-06-10

    Philips Azurion 7B12 Roadmap Pro may produce unusable dark images

    Philips Azurion 7B12/12 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 7B12/12, Model Numbers: 722067, 722225 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 (Devices)·Z-2307-2026·2026-06-10

    Aligned Medical fluids kits contain recalled lidocaine injection

    Aligned Medical AMS16835 Fluids Kits are being recalled because they include Lidocaine Hydrochloride Injection, USP that was recalled by a supplier for quality issues.

    Product
    Aligned Medical AMS16835 Fluids Kit RX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0579-2026·2026-06-10

    TopCare ultra strength antacid tablets contain small metallic particles

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

    Product
    TOPCARE ULTRA STRENGTH ANTACID ASSORTED FRUIT — TOPCARE ULTRA STRENGTH ANTACID ASSORTED FRUIT (CALCIUM CARBONATE)
    Category
    Drug
    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-0971-2026·2026-06-10

    Albertsons oatmeal raisin cookies do not declare almond allergen

    Albertsons store-made Oatmeal Raisin Cookies, 10 count, are being recalled because the contains statement does not declare almond. 62 units are affected.

    Product
    UPC 26911700000 COOKIES OATMEAL RAISIN 10CT 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-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 (Food)·H-1000-2026·2026-06-10

    Albertsons shrimp and surimi ceviche does not declare sea bream

    Albertsons store-made Shrimp & Surimi Ceviche Fresh is being recalled because the contains statement does not declare sea bream. 315 units are affected.

    Product
    UPC 23245700000 SHRIMP & SURIMI CEVICHE FRESH 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-1014-2026·2026-06-10

    Albertsons cajun seafood salad does not declare crab and pollock

    Albertsons store-made Cajun Seafood Salad is being recalled because the contains statement does not declare crab and pollock. 110 units are affected.

    Product
    UPC 29477800000 Ready Meals SALAD SEAFOOD CAJUN SS COLD UPC 29477600000 SALAD SEAFOOD CAJUN FS 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-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 (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 (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-0904-2026·2026-06-10

    Market of Choice vegan kale caesar salad has undeclared sesame

    Market of Choice Vegan Kale Caesar Salad is being recalled because sesame, a sub-ingredient of the za'atar spice, is not listed on the ingredients panel or contains statement.

    Product
    Market of Choice Vegan Kale Caesar Salad, Net Wt. 9.5oz. Finished product is pre-packaged into a clear flexible plastic clamshell container. Label has UPC 0 210126 01099 3. Market Central Kitchen 1150 Owen Loop S. Eugene, OR 97402 The Za'atar spice, which contains Sesame Seeds,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0995-2026·2026-06-10

    Albertsons imitation crab and shrimp salad does not declare pollock

    Albertsons store-made Imitation Crab and Shrimp Salad is being recalled because the contains statement does not declare pollock. 82 units are affected.

    Product
    UPC 23285300000 IMITATION CRAB AND SHRIMP SALAD 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-1037-2026·2026-06-10

    Albertsons turkey poppyseed salad does not declare almond allergen

    Albertsons store-made Kitchen Salad Turkey Poppyseed is being recalled because the contains statement does not declare almond.

    Product
    UPC 29361000000 KITCHEN SALAD TURKEY POPPYSEED SS COLD UPC 29360900000 KITCHEN SALAD TURKEY POPPYSEED FS COLD This is Albertson's store-made item and sold by random at point of sale with grocery store's scale label.
    Category
    Food
    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 (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-0906-2026·2026-06-10

    Raw Shelled Peanuts Recalled for Undeclared Tree Nut Allergen

    Wilco Peanut Co is recalling raw shelled peanuts (Runner Type) because they may contain undeclared tree nuts, posing an allergen risk to consumers with nut allergies.

    Product
    Raw Shelled Peanuts (Runner Type) 2,200 lb. Poly Tote Bags and 50kg Poly Bags
    Category
    Food
    Distribution
    4 states
  • 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-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
  • 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