The Recall Desk

State

Wisconsin product recalls

72,820 recalls have nationwide distribution and so reach Wisconsin. 8,407 additional recalls listed Wisconsin specifically in their distribution scope.

What the numbers show

Total
8,407
Critical
1,547
Severe
1,956
Most recent
2026-09-02

Of the 8,407 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 1,956 (23%) are Severe.

These figures cover only the 8,407 recalls whose distribution notice names Wisconsin specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

326–350 of 81227

  • HighCPSC·26692·2026-08-13

    COMMOWNER Electric Pressure Washers Recalled Over Shock and Electrocution Hazards

    COMMOWNER electric pressure washers (models HD14P-Z and HX18) are recalled due to shock and electrocution hazards from a missing built-in GFCI. No injuries reported; stop use and contact AZ Home Concept for a refund.

    Product
    COMMOWNER Electric Pressure Washers, model numbers HD14P-Z and HX18
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26702·2026-08-13

    Hampton Bay 52-Inch Ceiling Fans Recalled Over Blade Separation Hazard

    Hampton Bay Halwin 52-inch ceiling fans are being recalled because the fan blades can separate from the motor flywheel, posing impact and injury risks. About 9,460 units sold at Home Depot between January 2023 and October 2025 are affected.

    Product
    Hampton Bay Halwin 52-inch Indoor/Outdoor Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26689·2026-08-13

    TooyBing Wooden Bead Stacking Toys Recalled Due to Choking Hazard

    TooyBing is recalling its Wooden Bead Stacking Toys because the wooden beads pose a choking hazard to children under three years old.

    Product
    TooyBing Wooden Bead Stacking Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26690·2026-08-13

    DUMOS Nine-Drawer Dressers Recalled for Tip-Over and Entrapment Hazards

    DUMOS Nine-Drawer Dressers are recalled because they can tip over and entrap children if not anchored to the wall, violating the STURDY Act. Consumers should stop using unanchored units and contact DUMOS for a full refund.

    Product
    DUMOS Nine-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26699·2026-08-13

    SUGIFT Pressure Washers Recalled for Shock and Electrocution Hazards

    SUGIFT is recalling 13 electric pressure washers (Model LTBBHG006) because they lack a ground-fault circuit interrupter and have a short power cord, creating shock and electrocution risks. No injuries have been reported.

    Product
    SUGIFT Electric Pressure Washers, Model LTBBHG006
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V531000·2026-08-13

    Chrysler Recalls 2026-2027 Vehicles for Rearview Camera Display Failure

    Chrysler is recalling 2026-2027 Jeep, Ram, Chrysler, and Dodge vehicles because the rearview camera image may fail to display when reversing, increasing crash risk.

    Product
    RAM — RAM, CHRYSLER, JEEP PROMASTER BEV, PACIFICA, 2500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26698·2026-08-13

    CuberShop Magnetic Speed Cubes Recalled Over Magnet Ingestion Hazard

    CuberShop Magnetic Stickerless Speed Cubes (model YJ MGC 5×5) are recalled because loose high-powered magnets in the packaging pose an ingestion hazard to children. No injuries have been reported.

    Product
    CuberShop Magnetic Stickerless Speed Cubes, model YJ MGC 5×5
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V530000·2026-08-13

    GM Recalls 2024-2025 Silverado and Sierra 2500 Tires

    General Motors is recalling 2024-2025 Chevrolet Silverado 2500 and GMC Sierra 2500 trucks because incorrect tire pressure labels may cause underinflation and prevent low-pressure warnings.

    Product
    GMC — GMC, CHEVROLET SIERRA 2500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26697·2026-08-13

    Shengsen Prank Sound Makers Recalled Over Battery Ingestion Risk

    Shengsen Prank Sound Makers are recalled because the lithium coin batteries can be easily accessed by children, posing an ingestion hazard. About 667 units sold on Amazon from April 2024 through April 2026 are affected.

    Product
    Shengsen Prank Sound Maker
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0743-2026·2026-08-12

    Cyclophosphamide Injection Recalled Due to Stainless Steel Particulate Matter

    Sunny Pharmtech Inc. is recalling 4,077 vials of Cyclophosphamide for Injection due to stainless steel particulate matter found in the product. The recall affects vials distributed nationwide in the USA.

    Product
    Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2797-2026·2026-08-12

    Halyard Convenience Kits Recalled Due to Particulates in Manifolds

    AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.

    Product
    Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. SAMMC ANGIOGRAPHY SAMM066-15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2796-2026·2026-08-12

    Halyard convenience kits recalled due to potential particulates in manifolds

    AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.

    Product
    Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2854-2026·2026-08-12

    Copan WASPLab Software Recall Over Results Overwrite Issue

    Copan WASP is recalling WASPLab devices due to a software issue in the WebApp that may prevent users from overwriting results. The recall affects WebApp versions 2.33.1, 2.33.3, and 2.34.2.

    Product
    Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1, 2.33.3 and 2.34.2 Product Description: WASPLab is an automated device intended to be used for the incubation and the digital imaging of agar culture plates streaked w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2856-2026·2026-08-12

    Powered Wheelchair Control Software Recall by munevo

    Munevo is recalling 19 powered wheelchair hands-free control systems due to a software issue that may cause the driving mechanism to fall out of calibration, leading to unexpected steering drift or imprecise control.

    Product
    munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2840-2026·2026-08-12

    Radial Jaw 4 Jumbo Biopsy Forceps Packaging Sterile Barrier Recall

    Boston Scientific is recalling Radial Jaw 4 Jumbo Biopsy Forceps due to potential breach in the sterile barrier of device packaging. The recall affects 5,020 units in the US and 20,770 units outside the US.

    Product
    Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN: Radial Jaw 4 Jumbo 240cm Box 5; Outer Box UPN: M00513363; Inner Box UPN: M00513360.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2876-2026·2026-08-12

    GE Healthcare MAC VU360 Electrocardiograph Software Recall

    GE Healthcare is recalling 163 MAC VU360 electrocardiograph units due to a software issue that may cause a previous patient's data to remain visible and be incorrectly associated with a subsequent patient.

    Product
    GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2875-2026·2026-08-12

    Merge OrthoPACS Imaging Workstation Recall for Patient Data Display Issue

    Merge Healthcare is recalling 5 units of its Merge OrthoPACS medical imaging diagnostic workstation due to a software issue where thumbnails from a previously opened patient study may appear while a different patient study is currently open.

    Product
    Merge OrthoPACS, medical imaging diagnostic workstation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V526000·2026-08-12

    Nissan Recalls 2025 Altima Vehicles Due to Air Bag Fastener Defect

    Nissan is recalling 2025 Altima vehicles because incorrect mounting fasteners may prevent front passenger air bags from deploying as intended in a crash.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2862-2026·2026-08-12

    Stryker AHTO Tube Set Packaging Recalled for Handpiece Leaking

    Stryker is recalling 46,212 units of its AHTO Tube Set Packaging (Catalog Number 0250070600) due to reported complaints of leaking from the handpiece during use. The recall affects products distributed worldwide, including US Nationwide and multiple countries.

    Product
    STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2900-2026·2026-08-12

    GEM Premier 5000 PAK Lysing Solution Concentration Recall

    Specific lots of the GEM Premier 5000 PAK lysing bag solution have an active ingredient concentration that does not meet manufacturing specifications, which could delay recognition and management of Co-Oximetry and total bilirubin abnormalities.

    Product
    GEM Premier 5000 PAK Part Numbers: 00055360010 00055360011 00055407504 00055415010 00055430010 00055430011 00055445010 00055445011 00055360010.A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0744-2026·2026-08-12

    Cyclophosphamide Injection Recall: Stainless Steel Particulate Matter Found

    Cyclophosphamide for Injection, USP, 2 gram/vial, is being recalled due to the presence of particulate matter identified as stainless steel. The recall affects 1,464 vials distributed nationwide.

    Product
    Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8114-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2857-2026·2026-08-12

    OXOS Medical Recalls MC2 Portable X-Ray Systems Over Circuit Board Overheating

    OXOS Medical Inc is recalling 77 units of the MC2 Portable X-Ray System due to a defective circuit board that overheats. The recall affects devices distributed nationwide in FL, GA, IN, SC, TX, and VA.

    Product
    Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version: 5.7.0 Product Description: The MC2 Portable X-Ray System ( MC2 System or MC2 ) is a portable and handheld x-ray system designed to aid clinicians with po
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2909-2026·2026-08-12

    Blom-Singer Voice Prosthesis Boxes Mislabeled with Wrong Flange Type

    Freudenberg Medical is recalling 12 Blom-Singer Classic Indwelling Voice Prosthesis devices because the boxes are mislabeled, swapping Large Esophageal Flange and Large Esophageal and Tracheal Flange contents.

    Product
    Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm REF: 1610-LEF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2891-2026·2026-08-12

    Philips Allura X-Ray Systems Recalled Over Unauthorized Hard Disk Drives

    Philips is recalling 5,012 Allura interventional fluoroscopic X-ray systems nationwide due to potential loss of imaging functionality, motorized movement, or data caused by unauthorized hard disk drives.

    Product
    Philips Allura under the following System Descriptions and corresponding model numbers: 1. Allura Xper FD10; Model Numbers: 722003, 722010, 722026. 2. Allura Xper FD10 OR Table; Model Number: 722033. 3. Allura Xper FD10/10; Model Numbers: 722005, 722011, 722027. 4. Allura
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2897-2026·2026-08-12

    United Orthopedic U2 Knee Implant Bushings Recalled Over Engraving Design Issue

    United Orthopedic Corp. is recalling three Femoral offset bushing components of the U2 Total Knee System due to a design issue causing incorrect engraved numbering that could lead to incorrect implant orientation during surgery.

    Product
    Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 0mm and 4mm Model/Catalog Number: 9323-5310 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No, N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide