The Recall Desk

State

Wisconsin product recalls

72,907 recalls have nationwide distribution and so reach Wisconsin. 8,408 additional recalls listed Wisconsin specifically in their distribution scope.

What the numbers show

Total
8,408
Critical
1,547
Severe
1,957
Most recent
2026-09-09

Of the 8,408 recalls naming Wisconsin we have scored against our rubric, 1,547 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,957 (23%) are Severe.

These figures cover only the 8,408 recalls whose distribution notice names Wisconsin 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 81315

  • HighFDA (Devices)·Z-2274-2026·2026-06-10

    Ivenix infusion pump cassette loading levers may break

    The Large Volume Pump of the Ivenix Infusion System is being recalled because of the potential for the Cassette Loading Lever to break. 18,444 installed bases are affected.

    Product
    The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2286-2026·2026-06-10

    Philips Azurion 5M12 systems may show unusable dark fluoroscopy images

    Philips Azurion 5M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable.

    Product
    Philips Azurion 5M12, Model Numbers: 722227 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-0562-2026·2026-06-10

    Casey's extra strength antacid tablets contain small metallic particles

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

    Product
    Extra strength Antacid Calcium Carbonate 750 mg, chewable tablets, 96-count bottle, DISTRIBUTED BY CASEY'S MARKETING COMPANY, ANKENY, IA 50521, UPC: 0 98437 24361 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2262-2026·2026-06-10

    Baxter Exacta Mix inlet sets may contain incorrect 0.8-micron filters

    Exacta Mix Vented Micro-Volume Inlet tubing sets are being recalled because affected lots may contain 0.8-micron filters in place of the validated 3-micron filters.

    Product
    Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector Valve) and a spike or other appropriate connector on the opposite end to attach t
    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-0990-2026·2026-06-10

    Albertsons brie and bleu cheese tray does not declare almond

    Albertsons store-made Brie & Bleu Cheese Tray Large is being recalled because the contains statement does not declare almond. Eight units are affected.

    Product
    UPC 27841000000 Ready Meals TRAY BRIE & BLEU CHEESE LARGE 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 (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-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-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 (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-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 (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-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 (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 (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 (Drugs)·D-0571-2026·2026-06-10

    Hy-Vee extra strength antacid tablets contain small metallic particles

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

    Product
    HyVee, Extra Strength Antacid, Calcium Carbonate 750 mg, 96 CHEWABLE TABLETS, DISTRIBUTED BY: HY-VEE INC., Inc., WEST DES MOINES, IA 50266, UPC: 0 75450 82497 1.
    Category
    Drug
    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 (Food)·H-0893-2026·2026-06-10

    Straus Family Creamery vanilla bean ice cream may contain metal

    Straus Family Creamery Vanilla Bean Organic Super Premium Ice Cream in pints is being recalled over potential contamination with foreign objects, specifically metal pieces.

    Product
    STRAUS FAMILY CREAMERY Vanilla Bean ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100306
    Category
    Food
    Distribution
    17 states
  • 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-0897-2026·2026-06-10

    Straus Family Creamery mint chip ice cream may contain metal pieces

    Straus Family Creamery Mint Chip Organic Super Premium Ice Cream in pints is being recalled over potential contamination with foreign objects, specifically metal pieces.

    Product
    STRAUS FAMILY CREAMERY Mint Chip ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100504
    Category
    Food
    Distribution
    17 states
  • HighFDA (Food)·H-0961-2026·2026-06-10

    Cakerie strawberry shortcake triangles do not declare hazelnut allergen

    Albertsons store-made Cake Cakerie Strawberry Shortcake Triangle is being recalled because the contains statement does not declare hazelnut. 71 units are affected.

    Product
    UPC 25139500000 Cake Cakerie Strawberry Shortcake Triangle. 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-0557-2026·2026-06-10

    Kirkland Signature ultra strength antacid tablets contain metallic particles

    Kirkland Signature Ultra Strength Antacid, calcium carbonate 1000 mg, made by Guardian Drug Company for Costco, is being recalled over small metallic particles in the tablets.

    Product
    KIRKLAND ULTRA STREGTH ANTACID 171AB — KIRKLAND ULTRA STREGTH ANTACID 171AB (CALCIUM CARBONATE)
    Category
    Drug
    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