The Recall Desk

State

Minnesota product recalls

72,907 recalls have nationwide distribution and so reach Minnesota. 7,804 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,804
Critical
1,125
Severe
1,892
Most recent
2026-09-09

Of the 7,804 recalls naming Minnesota we have scored against our rubric, 1,125 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,892 (24%) are Severe.

These figures cover only the 7,804 recalls whose distribution notice names Minnesota 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 80711

  • 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 (Devices)·Z-2294-2026·2026-06-10

    Digital angiography and radiography systems may remain energized when switched off

    Digital angiography and radiography systems are being recalled because contactors in the high voltage generator may weld together, leaving the power supply energized when the system is off.

    Product
    Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D15
    Category
    Medical Device
    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-1020-2026·2026-06-10

    Albertsons chicken strip salad does not declare almond allergen

    Albertsons store-made Kitchen Salad Chicken Strip is being recalled because the contains statement does not declare almond. 55 units are affected.

    Product
    UPC 29433900000 Kitchen SALAD CHICKEN STRIP 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-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 (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-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-1032-2026·2026-06-10

    Albertsons pork meat pies do not declare anchovy allergen

    Albertsons store-made pork meat pies are being recalled because the contains statement does not declare anchovy. 790 units in total are affected.

    Product
    UPC 21176300000 MEAT PIE PORK 4CT SS COLD UPC 21025900000 PIE PORK 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-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 (Food)·H-1015-2026·2026-06-10

    Imitation Cajun crab seafood salad does not declare crab and pollock

    Albertsons store-made Seafood Salad Imitation Cajun Crab is being recalled because the contains statement does not declare crab and pollock. 53 units are affected.

    Product
    UPC 23114800000 SEAFOOD SALAD IMITATION CAJUN CRAB 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-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-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-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 (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 (Food)·H-0955-2026·2026-06-10

    Albertsons cravin carrot cake does not declare pecan allergen

    Albertsons store-made Cake Cravin Carrot 8-inch 1-layer is being recalled because the contains statement does not declare pecan. 138 units are affected.

    Product
    UPC 22679400000 CAKE CRAVIN CARROT 8IN 1-layer This is Albertson's store-made item and is sold by each unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1024-2026·2026-06-10

    Albertsons pad thai chicken meal does not declare anchovy

    Albertsons store-made Wok Pad Thai Chicken with Egg Roll is being recalled because the contains statement does not declare anchovy. 12 units are affected.

    Product
    UPC 21379600000 Ready Meals WOK PAD THAI CHICKEN WITH EGG ROLL 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-0565-2026·2026-06-10

    CareOne extra strength calcium antacid tablets contain metallic particles

    CareOne Extra Strength Calcium Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    EXTRA STRENGTH ANTACID — EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    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-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-2282-2026·2026-06-10

    Neptune docking station shipped without verified electrical safety testing

    A Neptune Smart Docking Station is being recalled because it was not released from manufacturing and may not have completed required testing, leaving a potential shock risk.

    Product
    Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
    Category
    Medical Device
    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-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-0985-2026·2026-06-10

    Albertsons pistachio muffins do not declare walnut allergen

    Albertsons store-made Pistachio Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 354 units are affected.

    Product
    UPC 22321200000 MUFFINS PISTACHIO 2CT UPC 22770600000 MUFFINS PISTACHIO 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-0559-2026·2026-06-10

    Tums assorted fruit antacid tablets contain small metallic particles

    Haleon Tums Antacid Assorted Fruit Tablets, 750 mg, in 330-count bottles are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 750 mg, 330-count bottle, Haleon, Warren, NJ 07059, UPC 3 0766 3072 10 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2300-2026·2026-06-10

    BD Pyxis Anesthesia Station 4000 fingerprint scanner may overheat

    The BD Pyxis Anesthesia Station 4000 is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.

    Product
    BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide