The Recall Desk

State

Wisconsin product recalls

73,584 recalls have nationwide distribution and so reach Wisconsin. 8,448 additional recalls listed Wisconsin specifically in their distribution scope.

What the numbers show

Total
8,448
Critical
1,557
Severe
2,309
Most recent
2026-10-24

Of the 8,448 recalls naming Wisconsin we have scored against our rubric, 1,557 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,309 (27%) are Severe.

Which agencies issued them

These figures cover only the 8,448 recalls whose distribution notice names Wisconsin specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23351–23375 of 82032

  • ModerateFDA (Drugs)·D-0749-2022·2022-04-13

    Sucralfate Oral Suspension Recalled Due to Label Mix-Up

    DASH Pharmaceuticals is recalling Sucralfate Oral Suspension nationwide due to a labeling mix-up affecting approximately 45,940 unit dose cups.

    Product
    Sucralfate Oral Suspension, USP 1g/10mL, packaged in a) 40 case of 10 mL unit Dose Cups (NDC 69339-148-17) and b) 100 case of 10 mL Unit Dose Cups (NDC 69339-148-19) Rx Only, Dash Pharmaceuticals, Upper Saddle River, NJ 07458.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0762-2022·2022-04-13

    Risedronate Sodium Tablets Recalled for Failed Content Uniformity Specifications

    Macleods Pharma USA Inc is recalling Risedronate Sodium 5 mg tablets (Lot BRD2001A, expiration 5/2022) due to failed content uniformity specifications. The recall affects 4,872 bottles distributed nationwide.

    Product
    RISEDRONATE SODIUM — RISEDRONATE SODIUM (RISEDRONATE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0770-2022·2022-04-13

    Ophthalmic drug recalled for subpotency and particulate matter

    Sun Pharmaceutical recalls CEQUA cyclosporine ophthalmic solution nationwide due to low assay results and particulate matter found in specific lots.

    Product
    CEQUA — CEQUA (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0888-2022·2022-04-13

    Brius Pontics Orthodontic Devices Recalled for Incomplete Design Validation

    Brius Technologies recalls Brius Pontics custom orthodontic devices that were sold before completing required design control procedures and documentation.

    Product
    Brius Pontics (components in a set of custom metal orthodontic devices);BRIUS , RX Only, Non-Sterile, Custom Made Device, ID: 52345400UL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0875-2022·2022-04-13

    Vena Cava Filter Sets Recalled for Instruction for Use Documentation Updates

    Cook Medical recalled 24,641 Gunther Tulip Vena Cava Filter Sets due to updates required in the Instruction for Use documentation covering device description, indications, contraindications, warnings, and precautions.

    Product
    Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Catalog Number/GPN: IGTCFS-65-1-FEM-TULIP G52917; IGTCFS-65-1-JUG-TULIP G52916; IGTCFS-65-1-UNI-TULIP G52918
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0752-2022·2022-04-13

    FDA Voluntary Recall of Methylprednisolone Tablets for Subpotency

    Jubilant Cadista Pharmaceuticals is recalling Methylprednisolone Tablets USP 4mg because they contain less active ingredient than labeled. Lot 21 P0322 was distributed nationwide and in Puerto Rico.

    Product
    Methylprednisolone Tablets, USP 4mg, 100-count bottle, Rx Only, Manufactured by: Jubliant Cadista Pharmaceuticals Inc. Salisbury, MD 21801, USA, NDC 59746-001-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0856-2022·2022-04-13

    Oral gel recalled for failed microbial testing

    SA3, LLC is recalling Silatrix Oral Gel Polymerized Sucralfate Gel due to failed microbial testing. Consumers should not use the product and contact their healthcare provider or SA3, LLC.

    Product
    Silatrix Oral Gel Polymerized Sucralfate Gel 10% (1 gm/10 gm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0889-2022·2022-04-13

    Brius Patient Specific Brackets recalled without completing design control process

    Brius Technologies is recalling Brius Patient Specific Brackets that were sold before the company completed the required design control process and regulatory documentation.

    Product
    Brius Patient Specific Brackets (components in a set of custom metal orthodontic devices); BRIUS , RX Only, Non-Sterile, Custom Made Device, ID: 52345400UL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0758-2022·2022-04-13

    Quinapril and Hydrochlorothiazide Tablets Recalled for Elevated Chemical Impurity

    Pfizer is recalling quinapril and hydrochlorothiazide tablets (20 mg/25 mg) nationwide due to elevated chemical impurities exceeding acceptable daily intake limits. No illnesses have been reported.

    Product
    quinapril and hydrochlorothiazide tablets, 20 mg/25 mg*, 90 Tablets bottles, Rx Only, Distributed by: Greenstone, LLC, Peapack, NJ, 07977, Made in Germany, NDC 59762-5225-9
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0730-2022·2022-04-13

    X-ray system displays incorrect collimation area information

    The YSIO X.Pree x-ray system's user interface displays incorrect collimation information during image acquisition. While actual collimation functions correctly, the display does not match preset parameters, potentially confusing operators.

    Product
    YSIO X.Pree
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0751-2022·2022-04-13

    Oral antiseptic rinse recalled due to label mix-up and wrong barcode

    The Natural Dentist Healthy Breath Antiseptic Rinse (Cool Mint) is being recalled due to a label mix-up. The back label incorrectly states the active ingredient as Peppermint Oil and Sage Oil and displays the wrong UPC code.

    Product
    The Natural Dentist Healthy Breath Antiseptic Rinse, Cool Mint, 16.9 FL OZ (500 mL, Manufactured for Revive Personal Products Company, Madison, NJ 07940, UPC Code 714132000714.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0745-2022·2022-04-13

    Sodium Chloride Injection with Incorrect Barcode Labeling Recalled Nationwide

    Ritedose is recalling 3,795 prefilled syringes of sodium chloride injection nationwide. The barcodes incorrectly identify the product as rocuronium bromide, creating a medication identification risk in healthcare settings.

    Product
    23.4% Sodium Chloride Injection, 120 mEq per 30 mL (4 mEq/mL), 50 mL prefilled syring, Rx Only, RITEDOSE, 503B Outsourcing Facility, A Division of the RITEDOSE Corporation, 1 Technology Circle, Columbia, SC 29203, 1-866-994-4670, NDC: 65302-509-30, barcode N (01) 003 65302 50930…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0876-2022·2022-04-13

    Cook Celect Platinum Vena Cava Filter Set Instructions Recall

    Cook Medical is recalling Celect Platinum Vena Cava Filter Sets due to revisions needed in the instructions for use, including updates to contraindications, warnings, precautions, and potential adverse events.

    Product
    Cook Celect PlatinumVena Cava Filter Set Catalog Number/GPN: IGTCFS-65-1-FEM-CELECT-PT G34502; IGTCFS-65-1-JUG-CELECT-PT G34309; IGTCFS-65-1-UNI-CELECT-PT G34505;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V235000·2022-04-12

    Tesla Model S Boombox function obscures pedestrian warning system sounds

    Tesla is recalling certain 2020-2022 Model S, X, Y and 2017-2022 Model 3 vehicles. The Boombox feature can obscure Pedestrian Warning System sounds while driving. A free software update will disable Boombox in Drive, Neutral, and Reverse modes.

    Product
    TESLA — TESLA MODEL X, MODEL 3, MODEL Y, MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V236000·2022-04-12

    Prevost Recalls 2018 X3-45 Buses Due to Frayed Seat Belt Wires

    Prevost is recalling 2018 X3-45 buses because frayed seat belt wires may prevent buckles from working properly, increasing injury risk in crashes.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V234000·2022-04-11

    Newmar RVs recalled for unsecured seat wiring fire risk

    Newmar is recalling multiple 2019–2022 RV models due to unsecured wiring beneath seats that can cause electrical short circuits and fire. Owners should contact their dealer for free inspection and repair.

    Product
    NEWMAR — NEWMAR CANYON STAR, BAY STAR SPORT, BAY STAR, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V233000·2022-04-08

    2021-2022 Tesla Model X Side Curtain Air Bag Deployment Defect

    Tesla is recalling certain 2021-2022 Model X vehicles due to a defect in the left or right front-row side curtain air bags that may not deploy properly when windows are lowered. Improper deployment increases the risk of injury during crashes.

    Product
    TESLA — TESLA MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V229000·2022-04-08

    Big Tex Recalls 2022 Trailers Due to Improperly Welded Couplers

    Big Tex Trailer Manufacturing is recalling 2022 50SR and 70SR trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle.

    Product
    BIG TEX — BIG TEX 70SR, 50SR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V231000·2022-04-08

    Mercedes-Benz Recalls 21,306 Vehicles for Electrical Fire Risk

    Mercedes-Benz is recalling 21,306 vehicles because a ground cable bolt may not be secured properly, which can cause the electrical cable to overheat and increase the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS 450 4MATIC, AMG GLE53, GLE 450, GLE 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22C001000·2022-04-08

    CYBEX Sirona M Child Seat Recall for Foam Choking Hazard

    Columbus Trading-Partners USA is recalling CYBEX Sirona M child seats because loose foam pieces from the headrest pad may pose a choking hazard to children.

    Product
    CHILD SEAT:MATERIAL/PADDING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V232000·2022-04-08

    Mercedes-Benz 2018-2021 models recalled for rearview camera display failure

    Mercedes-Benz is recalling 126,443 vehicles from 2018-2021 because the rearview camera display may fail to show the rear view due to a software error, reducing visibility and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLB35, GLB 250, AMG CLA45, AMG CLA35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V230000·2022-04-08

    Western Star trucks recalled for failing windshield wiper linkages

    Daimler Trucks North America is recalling certain 2020-2022 Western Star 49X and 2021 Western Star 47X vehicles because windshield wiper linkages may break, causing wipers to fail and reducing visibility.

    Product
    WESTERN STAR — WESTERN STAR 47X, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22739·2022-04-07

    Bestar Wall Beds Recalled Due to Detachment and Crush Hazards

    Bestar wall beds can detach from the wall and fall, creating impact and crush hazards. One death and 60 additional injuries have been reported.

    Product
    Bestar Wall Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide