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.

6151–6175 of 81392

  • HighNHTSA·25V496000·2025-07-31

    Premier Trailer Recalls 2024 Reel and Pole Trailers Due to Brake Oil Leak

    Premier Trailer Solutions is recalling 2024 Reel and Pole trailers because improperly installed oil seals may leak oil onto the brake system, reducing braking ability.

    Product
    PREMIER TRALER — PREMIER TRALER POLE TRAILER, REEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25416·2025-07-31

    RIDGID brushless framing nailers can discharge a nail from the trigger alone

    RIDGID 18Volt Brushless 21-Degree and 30-Degree Framing Nailers are being recalled because the dual action engagement system can malfunction and involuntarily discharge a nail. About 64,000 units affected.

    Product
    RIDGID 18Volt Brushless 21-Degree Framing Nailers and RIDGID 18Volt Brushless 30-Degree Framing Nailers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V498000·2025-07-31

    Storyteller Overland Recalls 2023 Mode LT RVs Due to Shore Power Fire Risk

    Storyteller Overland is recalling 2023 Mode LT recreational vehicles because improperly tightened shore power inlets may overheat and cause a fire. Dealers will replace the inlets free of charge.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND MODE LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25414·2025-07-31

    Leatherman Charge Plus multi-tool knife blades do not fully fold in

    Leatherman Charge Plus and Charge Plus TTi multi-tools are being recalled because the tip of the knife blade does not fully fold into the handle, posing a laceration hazard. About 17,000 units affected.

    Product
    Leatherman Charge Plus and Charge Plus TTi Multi-Tools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2165-2025·2025-07-30

    Biofinity XR Toric contact lens blisters may have a leaking seal

    Biofinity XR Toric Contact Lenses are being recalled because lens blisters may have an incomplete or leaking seal, which may render them unsterile. 397 units are affected.

    Product
    Biofinity XR Toric Contact Lens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0323-2025·2025-07-30

    Ritz peanut butter cracker 20 count cartons recalled over undeclared peanut

    Ritz Peanut Butter Cracker Sandwiches in 27.6 oz 20 count cartons are being recalled because of undeclared peanut allergens due to mispackaging. 24,446 cases are affected.

    Product
    Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside cartons. And 6x20(6 - 27.6 oz Cartons) in master carton. UPC 1 00 44000 07584 2
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-2135-2025·2025-07-30

    HSG procedure trays label non-sterile iodine pouches as sterile

    HSG Procedure Trays are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 171 units are affected.

    Product
    HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and sonohysterography procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2151-2025·2025-07-30

    Nellcor bedside SpO2 monitor alarms may not be heard or recognized

    The Covidien Nellcor Bedside SpO2 Patient Monitoring System is being recalled because alarms may not be heard or recognized, which the manufacturer links to treatment delay. 264,790 units are affected.

    Product
    Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N, 10005941-SG, DS10005941, 10005941J, 10005941JP, 10005941JPN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V497000·2025-07-30

    Brinkley trailer wiring may be unsecured risking a short circuit

    Brinkley RV is recalling certain 2025 Model Z trailers because the electrical wiring may not be secured properly, which can damage the wiring and cause a short circuit.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2130-2025·2025-07-30

    SIGNA Architect gradient coils can produce acoustic noise above the limit

    GE HealthCare SIGNA Architect MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    SIGNA Architect
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2171-2025·2025-07-30

    Stryker StrykeFlow irrigator with tip may leak solution into handpiece

    The Stryker StrykeFlow Disposable Suction/Irrigator with Disposable Tip is being recalled because irrigation solution may leak into the handpiece and battery pack, causing it to malfunction.

    Product
    Stryker, StrykeFlow REF: 0250070520 / 2, Disposable Suction/Irrigator with Disposable Tip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-07302025-01·2025-07-30

    Frozen Pork and Beef Tortellini Recalled for Undeclared Soy and Sesame Allergens

    USDA FSIS issued a public health alert for frozen tortellini that may contain undeclared soy and sesame. Consumers with allergies should not consume the product.

    Product
    P.E. & F Inc. DBA DiMare's Specialty Foods — FSIS Issues Public Health Alert for Frozen Pork and Beef Tortellini Product Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2168-2025·2025-07-30

    SmartSync Patient Connector limited the window to abort high voltage therapy

    The Medtronic CareLink SmartSync Patient Connector is being updated because in prior application versions the abort window during an induction test limited the user's ability to cancel high voltage therapy. 22,091 devices affected.

    Product
    Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Crome application, Software Model Number D00U005; 2. Claria Amplia Compia application, Software Model Number D00U009; 3. Evera MRI application, Software M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2166-2025·2025-07-30

    Biofinity Toric Multifocal contact lens blisters may have a leaking seal

    Biofinity Toric Multifocal Contact Lenses are being recalled because lens blisters may have an incomplete or leaking seal, which may render them unsterile. 827 units are affected.

    Product
    Biofinity Toric Multifocal Contact Lens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2132-2025·2025-07-30

    Discovery MR750w gradient coils can produce acoustic noise above the limit

    GE HealthCare Discovery MR750w 3.0T MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    Discovery MR750w 3.0T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2133-2025·2025-07-30

    SIGNA PET/MR gradient coils can produce acoustic noise above the limit

    GE HealthCare SIGNA PET/MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    SIGNA PET/MR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0319-2025·2025-07-30

    Artisan style half loaves recalled over undeclared hazelnut from mispackaging

    Artisan Style 1/2 Loaf white bread is being recalled because product containing hazelnuts was put in bags whose allergen statement does not include hazelnuts. 883 loaves are affected.

    Product
    Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/2 Loaf of white bread with white flour topping and two splits on top 7/13/2025 - Best By Flexible plastic bag
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·H-0324-2025·2025-07-30

    Ritz peanut butter cracker 40 count cartons recalled over undeclared peanut

    Ritz Peanut Butter Cracker Sandwiches in 55.2 oz 40 count cartons are being recalled because of undeclared peanut allergens due to mispackaging. 224 cases are affected.

    Product
    Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 count (40x1.38 oz 6 pack of cracker sandwiches inside carton. 40 - 55.2oz Cartons in master carton. UPC 0 44000 07819 5
    Category
    Food
    Distribution
    49 states
  • HighFDA (Food)·H-0326-2025·2025-07-30

    Ritz peanut butter cracker sandwiches recalled over undeclared peanut from mispackaging

    Ritz Peanut Butter Cracker Sandwiches are being recalled because of undeclared peanut allergens due to mispackaging. 37,985 units are affected across nearly every state.

    Product
    Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 count (8x1.38 oz 6 pack of cracker sandwiches inside carton. 14X8-Case: 14 - 11.04 Oz Cartons in master carton. UPC 0 44000 88210 5
    Category
    Food
    Distribution
    49 states
  • HighFDA (Drugs)·D-0541-2025·2025-07-30

    Budesonide inhalation ampoules recalled after leakage and empty ampoule complaint

    Budesonide Inhalation Suspension 0.5 mg/2 mL is being recalled for lack of assurance of sterility after a market complaint was received for leakage and an empty ampoule. 13,680 ampoules affected.

    Product
    BUDESONIDE — BUDESONIDE (BUDESONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2162-2025·2025-07-30

    BD COR system software issue could produce possible false negative results

    BD COR System Software version 8.80 and above is being recalled because of a potential functionality issue supporting the Over labeling feature that could lead to possible false negative results. 7 systems affected.

    Product
    BD COR System Software. Model Number: 444829.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0535-2025·2025-07-30

    Compounded epinephrine lidocaine vials returned subpotent assay results in stability testing

    Epinephrine Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL vials compounded by Imprimis NJOF are being recalled because of subpotent assay results during stability testing. 6,880 vials affected.

    Product
    Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 07852 NDC: 71384-641-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2170-2025·2025-07-30

    Stryker StrykeFlow suction irrigator may leak solution into the handpiece

    The Stryker StrykeFlow Disposable Suction/Irrigator is being recalled because irrigation solution may leak into the handpiece and battery pack, causing it to malfunction.

    Product
    Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2131-2025·2025-07-30

    SIGNA Architect AIR gradient coils can produce acoustic noise above limit

    GE HealthCare SIGNA Architect AIR MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    SIGNA Architect AIR
    Category
    Medical Device
    Distribution
    Distributed nationwide