The Recall Desk

State

Wisconsin product recalls

72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3376–3400 of 81344

  • HighCPSC·26267·2026-02-12

    Adult portable bed rails recalled over entrapment and asphyxiation risk

    About 800 Beloems-branded adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.

    Product
    Beloems Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26263·2026-02-12

    Fortemotus bed rails recalled over entrapment and asphyxiation risk

    About 550 Fortemotus-branded adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.

    Product
    Fortemotus Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26266·2026-02-12

    Baby bath seats recalled over instability that can cause drowning

    About 590 CheerKid baby bath seats are being recalled because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.

    Product
    CheerKid Baby Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26260·2026-02-12

    Smoke alarms recalled because they may not sound in time

    About 11,000 3-Pack Smoke Detector Fire Alarms are being recalled because if the sensing threshold is set too high, the alarm might not sound in a timely manner.

    Product
    3-Pack Smoke Detector Fire Alarms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V084000·2026-02-12

    International truck software may fail to brake with adaptive cruise

    International is recalling certain 2026-2027 MV vehicles because the ECU software may fail to engage the brakes when adaptive cruise control or hill hold assist is in use.

    Product
    INTERNATIONAL — INTERNATIONAL MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26268·2026-02-12

    Spa hydromassage jets recalled over hair entanglement and drowning hazards

    About 32,900 hydromassage rotary jets in Highlife Collection spas are being recalled because the suction force can entangle a user's hair and submerge their head underwater.

    Product
    Hydromassage Rotary Jet (6 fin) in Highlife Collection spas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26265·2026-02-12

    Magnetic board games recalled over loose high-powered magnet pieces

    About 1,200 Colombia-themed magnetic board games are being recalled because the magnetic game pieces contain loose high-powered magnets, posing an ingestion hazard to children.

    Product
    Colombia-themed Magnetic Board Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0304-2026·2026-02-11

    Male supplement capsules recalled after FDA analysis found tadalafil

    Green Lumber Holdings is recalling Green Lumber Natural Fuel For Men capsules because FDA analysis found the product to contain tadalafil, and it is marketed without an approved application.

    Product
    Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San Miguel Drive, Suite #296, Newport Beach, CA 92660
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1163-2026·2026-02-11

    HOT AXIOS 20mm stents recalled over deployment and expansion problems

    Boston Scientific is recalling 588 units of the HOT AXIOS Stent and Electrocautery-Enhanced Delivery System, 20mm x 10mm after increased reports of stent deployment and expansion issues.

    Product
    *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm; Material Number (UPN): M00553560;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1159-2026·2026-02-11

    AXIOS 6mm stents recalled over deployment and expansion problems

    Boston Scientific is recalling 39 AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 6mm x 8mm, after increased reports of stent deployment and expansion issues.

    Product
    AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm; Material Number (UPN): M00553680;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0499-2026·2026-02-11

    Spice cake mix recalled over an undeclared milk allergen

    B.C. Williams Bakery Service is recalling 51 bags of Spice Cake Mix, sold in 50 lb bags, over an undeclared milk allergen.

    Product
    Spice Cake Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0500-2026·2026-02-11

    Bread and roll mix recalled over an undeclared milk allergen

    B.C. Williams Bakery Service is recalling 720 bags of Bread and Roll Mix, sold in 50 lb bags, over an undeclared milk allergen.

    Product
    Bread and Roll Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1160-2026·2026-02-11

    AXIOS 8mm stents recalled over deployment and expansion problems

    Boston Scientific is recalling 59 units of the AXIOS Stent and Electrocautery-Enhanced Delivery System, 8mm x 8mm after increased reports of stent deployment and expansion issues.

    Product
    AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm; Material Number (UPN): M00553690;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1161-2026·2026-02-11

    HOT AXIOS stents recalled over deployment and expansion problems

    Boston Scientific is recalling 266 HOT AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 6mm x 8mm, after increased reports of stent deployment and expansion issues.

    Product
    HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 6mm x 8mm; Material Number (UPN): M00553520;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0481-2026·2026-02-11

    Bread crumbs recalled over undeclared egg and milk allergens

    VH Foods is recalling 4,497 packages of Outside The Breadbox brand Bread Crumbs, 8 oz, over undeclared egg and milk.

    Product
    Bread Crumbs, Outside The Breadbox brand, net wt. 8 oz, UPC 873799001554. Product is packaged in a clear stand up pouch. Intended use baking. Condition/Shelf Life shelf stable, 180 days. Firm name Outside The Breadbox, 2027 W Colorado Ave. Colorado Springs, CO.
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Devices)·Z-1162-2026·2026-02-11

    HOT AXIOS 8mm stents recalled over deployment and expansion problems

    Boston Scientific is recalling 150 HOT AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 8mm x 8mm, after increased reports of stent deployment and expansion issues.

    Product
    *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm; Material Number (UPN): M00553530;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1158-2026·2026-02-11

    AXIOS stents recalled over deployment and expansion problems during placement

    Boston Scientific is recalling 557 AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 20mm x 10mm, after increased reports of stent deployment and expansion issues.

    Product
    AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm; Material Number (UPN): M00553660;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0501-2026·2026-02-11

    Swiss chocolate cake mix recalled over an undeclared milk allergen

    B.C. Williams Bakery Service is recalling 95 bags of Swiss Chocolate Cake Mix, sold in 50 lb bags, over an undeclared milk allergen.

    Product
    Swiss Chocolate Cake Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V081000·2026-02-11

    Nissan Rogue electronic throttle body gears may break during driving

    Nissan is recalling certain 2024-2025 Rogue vehicles with the 1.5L VC-Turbo engine because the gears in the electronic throttle body assembly may break, causing a loss of drive power.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V080000·2026-02-11

    Nissan Rogue turbo engine bearings may seize causing engine failure

    Nissan is recalling certain 2023-2025 Rogue vehicles with the 1.5L VC-Turbo engine because increased temperatures can break down the engine oil, causing the bearings to seize and the engine to fail.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0477-2026·2026-02-11

    Five blend sea moss gel recalled over potential Clostridium botulinum

    Diva Fam is recalling Sea Moss Gel Superfood in the 5 Blend in 1 variety over potential Clostridium botulinum contamination.

    Product
    Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. 5 Blend in 1- UPC# 5061033690052
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1265-2026·2026-02-11

    Vivoo protein tests recalled over missing FDA premarket clearance

    Changchun Wancheng Bio-Electron is recalling 500 units of the Vivoo Protein Test because tests requiring a 510(k) were distributed before they could be legally marketed.

    Product
    Vivoo Protein Test
    Category
    Medical Device
    Distribution
    Distributed nationwide