The Recall Desk

State

Wisconsin product recalls

72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6326–6350 of 81392

  • HighNHTSA·25V464000·2025-07-11

    Forest River Recalls 2026 Westbrook and Tracer Trailers for LP Gas Hose Defect

    Forest River is recalling 2026 Westbrook and Tracer recreational trailers because a liquid propane gas hose may rub against the furnace, causing a fuel leak that increases fire risk.

    Product
    FOREST RIVER — FOREST RIVER WESTBROOK, TRACER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V463000·2025-07-11

    Mercedes-Benz Metris rearview camera image may fail to display

    Daimler Vans USA is recalling certain 2020-2023 Mercedes-Benz Metris vehicles because unsecured infotainment connections can stop the rearview camera image displaying. 43,422 vehicles affected.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25377·2025-07-10

    Ozark Trail 64 ounce water bottle lids can forcefully eject

    Ozark Trail 64 oz Stainless Steel Insulated Water Bottles are being recalled because the lid can forcefully eject on opening. Three injuries are reported, including two cases of permanent vision loss.

    Product
    Ozark Trail 64 oz Stainless Steel Insulated Water Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V462000·2025-07-10

    Mitsubishi Fuso Rizon Trucks Recalled for Electric Parking Brake Fire Risk

    Mitsubishi Fuso is recalling 2024-2025 Rizon trucks because an oversized spacer in the electric parking brake may cause overheating and fire.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO RIZON FEC7K (E16), RIZON FEC9K (E18), RIZON FECXK (E18)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25384·2025-07-10

    AUGNORYE padded crib bumpers recalled under the federal crib bumper ban

    AUGNORYE padded cushioned crib bumpers are being recalled because they violate the federal crib bumper ban and can obstruct an infant's breathing. About 356 units are affected.

    Product
    AUGNORYE Padded Cushioned Crib Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25383·2025-07-10

    Braided crib bumpers recalled under the federal crib bumper ban

    Unbranded braided crib bumpers are being recalled because they violate the federal crib bumper ban and can obstruct breathing. About 260 units are affected.

    Product
    Braided crib bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25380·2025-07-10

    WLIVE fabric 15-drawer dressers recalled over tip-over and entrapment hazards

    WLIVE Fabric 15-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the federal standard under the STURDY Act. About 6,600 units affected.

    Product
    WLIVE Fabric 15-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25379·2025-07-10

    Creekliybear play yard mattresses recalled over entrapment and suffocation hazard

    Creekliybear "Pack and Play" aftermarket play yard mattresses are being recalled because they exceed thickness requirements and may not fit certain play yards. About 21,500 units affected.

    Product
    Creekliybear "Pack and Play" Aftermarket Play Yard Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0505-2025·2025-07-09

    Zicam Nasal AllClear swabs recalled over fungal contamination of swabs

    Zicam Nasal AllClear swabs are being recalled because of fungal contamination of the nasal swabs. All lots are affected, covering 13,632 cartons.

    Product
    ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc.., Ewing NJ. UPC 7 32216 30165 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0207-2025·2025-07-09

    Fruit and Vegetable Trays Recalled for Potential Salmonella Contamination

    JFE Franchising Inc. is recalling multiple fruit and vegetable tray products because cucumbers may be contaminated with Salmonella. The affected products were distributed in seven states with a sell-by date of May 20, 2025.

    Product
    Fruit & Vegetable Tray - 64 oz 63912394047 Mixed Melon, Cucumbers & Tajin - 18oz 63912394007 Watermelon & Cucumber w/ Tajin - 18oz 63912394036 Small Vegetable Tray - 19.5 oz 63912388045 Small Party Tray with Dip - 19 oz 63912388046 Large Vegetable Tray - 42 oz 63912
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-2014-2025·2025-07-09

    Servo-n ventilators may measure patient circuit compliance inaccurately

    The Servo-n Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 7,688 units affected.

    Product
    Servo-n Ventilator System. Model Number: 6694800.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2041-2025·2025-07-09

    HardyCHROM CRE Culture Medium Recalled for Quality Control Failure

    Hardy Diagnostics is recalling HardyCHROM CRE culture medium (Catalog No. G323) distributed across 22 US states and Puerto Rico. The product failed quality control testing due to breakthrough growth of Klebsiella pneumoniae.

    Product
    HardyCHROM CRE, selective and differential culture medium for antimicrobial susceptibility testing, Product Catalog No. G323
    Category
    Medical Device
    Distribution
    22 states
  • SevereFDA (Drugs)·D-0570-2025·2025-07-09

    Buffered penicillin G potassium vials may actually contain cefazolin for injection

    Buffered Penicillin G Potassium for Injection is being recalled because some vials of cefazolin for injection were incorrectly labeled as penicillin G potassium 20 million units.

    Product
    PENICILLIN G POTASSIUM — PENICILLIN G POTASSIUM (PENICILLIN G POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0503-2025·2025-07-09

    Lidocaine HCL Sterile Injection recalled for sterility assurance concerns

    Tailstorm Health INC is recalling Lidocaine HCL Sterile Injection (20 mg/mL) due to FDA inspection findings of concerns with the sterile manufacturing process. The recalled product is distributed nationwide.

    Product
    LIDOcaine HCL Sterile Injection, USP, 20 mg/mL, 2%, (200 mg/10 mL), For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative Free, 10mL Sterile Single-Dose Vial, Rx Only, Medivant Healthcare, 158 S. Kyrene Rd., Chandler, AZ, 85226, NDC 81483-0001-0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2015-2025·2025-07-09

    Servo-u MR Ventilator System inaccurate patient circuit compliance measurement

    Servo-u MR Ventilator System (Model 6888800) may measure patient circuit compliance inaccurately due to incorrect pre-use leakage testing and incorrect active humidifier use.

    Product
    Servo-u MR Ventilator System. Model Number: 6888800.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0504-2025·2025-07-09

    Zicam cold remedy nasal swabs recalled over fungal contamination

    Zicam Cold Remedy Medicated Nasal Swabs are being recalled because of fungal contamination of the swabs. All lots are affected, covering 3,374,918 cartons.

    Product
    ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0208-2025·2025-07-09

    Bibimbap Bowl recalled due to potential Salmonella contamination

    JFE Franchising Inc is recalling 13 oz Bibimbap Bowls (UPC 63912389259) because cucumbers in the product have the potential to be contaminated with Salmonella.

    Product
    Bibimbap Bowl 13 oz 63912389259
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-2013-2025·2025-07-09

    Servo-u ventilators may measure patient circuit compliance inaccurately

    The Servo-u Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 874 units are affected.

    Product
    Servo-u Ventilator System. Model Number: 6688600.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2048-2025·2025-07-09

    Philips Ultrasound Transducers Recalled After Over-Refurbishment

    Philips Ultrasound, Inc is recalling 5,230 Philips 3D9-3v Transducer devices because they were refurbished beyond their useful life, posing a risk of device failure during medical use.

    Product
    Philips 3D9-3v Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0206-2025·2025-07-09

    Fresh cut cucumber products recalled over potential Salmonella contamination

    Fresh cut cucumber products from JFE Franchising, including cucumber with ranch and cucumber with Tajin, are being recalled because the cucumbers may be contaminated with Salmonella.

    Product
    Cucumber with Ranch - 9 oz 63912395020 Cucumber, Lime & Tajin - 19oz 63912388053 Cucumber Slices w/Tajin - 15 oz 63912388022 Cucumber Bowl w/ Ranch Dressing - 15 oz 63912388063
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0506-2025·2025-07-09

    Orajel Baby teething swabs recalled over fungal contamination of swabs

    Orajel Baby Cooling Swabs for Teething are being recalled because of fungal contamination of the infant oral swabs. All lots are affected, covering 695,880 cartons.

    Product
    Orajel Baby, Cooling Swabs for Teething, Each Unit 0.007 fl oz (0.22 mL), NET 0.08 FL OZ (2.6 mL) TOTAL, 12 Single-Use Swabs per carton, Manufactured for Church & Dwight Co. Inc. Ewing. NJ 08328 USA. UPC CODE 3 10310 40000 2.
    Category
    Drug
    Distribution
    Distributed nationwide