The Recall Desk

State

Minnesota product recalls

73,833 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,851
Critical
1,137
Severe
2,246
Most recent
2026-11-04

Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58676–58700 of 81684

  • HighNHTSA·15V520000·2015-08-17

    BMW Recalls 3-Series Vehicles Due to Inoperative Side Marker Lights

    BMW is recalling certain 2012-2015 3-Series vehicles because software may cause front side marker lights to fail, reducing visibility at night.

    Product
    BMW — BMW 328XI, 328XD, 328I, 328D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V517000·2015-08-14

    Chrysler Recalls 2014-2015 Ram 1500 Diesel Trucks for Fire Risk

    Chrysler is recalling 2014-2015 Ram 1500 diesel trucks because a battery harness may rub against the frame, causing an electrical short that could lead to stalling or fire.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·111-2015·2015-08-14

    Pleasant House Bakery Recalls Steak and Chicken Pies for Undeclared Allergens

    Pleasant House Bakery is recalling steak and chicken pies distributed without inspection and containing undeclared eggs, milk, and wheat.

    Product
    Pleasant House Bakery Recalls Steak and Chicken Products Distributed Without the Benefit of Inspection and Due to Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E065000·2015-08-14

    Marmon-Herrington Recalls Drive Axles with Improperly Tightened Hex Nuts

    Marmon-Herrington is recalling specific drive axles manufactured between July 2014 and July 2015 because hex nuts may not be properly tightened, posing a crash risk.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15746·2015-08-14

    Trane and American Standard Recall Accessory Heaters Due to Fire Hazard

    Trane and American Standard are recalling specific accessory heaters installed in air handlers due to a fire hazard caused by overheating.

    Product
    Accessory heaters installed in TAM7 and TAM8 air handlers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V519000·2015-08-14

    GM Recalls Vehicles for Headlamp Driver Module Overheating Defect

    General Motors is recalling specific 2005-2009 models because the headlamp driver module may overheat and fail, causing lights to stop working.

    Product
    SAAB — SAAB, BUICK, PONTIAC 9-7X, LACROSSE, RAINIER, GRAND PRIX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V516000·2015-08-13

    Pierce Emergency Vehicles Recalled for Driveshaft Defect

    Pierce is recalling 2014-2015 emergency vehicles because a driveshaft may bend or twist, potentially causing loss of drive and road hazards.

    Product
    PIERCE — PIERCE DASH CF, ENFORCER, VELOCITY, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V512000·2015-08-13

    Terex Recalls 2013-2015 Digger Derrick and Aerial Devices Trucks

    Terex is recalling 386 model year 2013-2015 Digger Derrick and Aerial Devices trucks because vertical cylinders may drift when loaded, risking platform falls.

    Product
    TEREX — TEREX DIGGER DERRICK, AERIAL DEVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15213·2015-08-13

    Ambient Weather Recalls Radios Due to Fire Hazard

    Ambient Weather is recalling about 12,500 weather radios because the AC power adapter can overheat, posing a fire hazard. Consumers should stop using the radios and contact the company for a free replacement adapter.

    Product
    Ambient Weather radios
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V515000·2015-08-13

    Toyota Recalls 4Runners Due to Accessory Exhaust Tip Burn Risk

    Southeast Toyota Distributors is recalling 2010-2015 Toyota 4Runners because accessory exhaust tips may contact people and cause burns.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V513000·2015-08-13

    AEV Trauma Hawk Recalled for Reversed Backup Camera Images

    Halcore Group is recalling 2014-2015 AEV Trauma Hawk emergency vehicles because the backup camera may display reversed images, increasing crash risk.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2936-2015·2015-08-12

    Supervalu Danish Rolls Recalled for Undeclared Milk Allergen

    Supervalu, Inc. is recalling Danish Rolls that may contain undeclared milk. The product was distributed in Minnesota and Illinois.

    Product
    Danish Rolls, 4 Ct., Net Wt. 13oz. in clear plastic clam shell.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2319-2015·2015-08-12

    Cook Inc. Recalls Slip-Cath Beacon Tip Catheters Due to Tip Separation

    Cook Inc. is recalling Slip-Cath Beacon Tip Catheters because the tips may split or separate, potentially causing loss of function or complications.

    Product
    Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2943-2015·2015-08-12

    Anabolic Science Labs Recalls Slim X Lean Hour Energy Drink

    Anabolic Science Labs is recalling Slim X Lean Hour 12+ Hour Energy products due to undeclared synthetic hormone ingredients.

    Product
    "***SLIM X LEAN HOUR 12+ HOUR ENERGY***PRODUCT ID: ASL-SXL-03***Manufactured for: ASL ANABOLIC SCIENCE LABS WINTER PARK, FL 32789***
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2318-2015·2015-08-12

    Cook Inc. Recalls Beacon Tip Royal Flush Plus High-Flow Catheters

    Cook Inc. is recalling Beacon Tip Royal Flush Plus High-Flow Catheters due to reports of tip splits or separation that may cause loss of function or complications.

    Product
    Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2325-2015·2015-08-12

    Medtronic Passive Biopsy Needle Kit Recalled for Adhesive Defect

    Medtronic is recalling 1,415 Passive Biopsy Needle Kits because adhesive failure may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.

    Product
    Medtronic Passive Biopsy Needle Kit, Part Number 9731754 - Passive Biopsy Fee Per Use (FPU) Kit. The image guided Passive Biopsy Needle is an accessory instrument with the StealthStation System. The Biopsy Needle is intended to be used for stereotaxy biopsy of brain tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2326-2015·2015-08-12

    Aesculap S4C Occiput Torque Wrench Recalled Due to Reassembly Defect

    Aesculap is recalling 10 S4C Occiput Torque Wrenches because improper reassembly after reprocessing caused a screw to break during implantation.

    Product
    S4C Occiput Torque Wrench F/Set Screw; used to tighten the S4 Cervical Spinal System clamping screws with a defined torque 2.8 Nm for tightening the clamping screw in the screw head/hook head/occipital plate/transverse connector and other connectors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2317-2015·2015-08-12

    Cook Inc. Recalls Beacon Tip Torcon NB Advantage Catheters

    Cook Inc. is recalling Beacon Tip Torcon NB Advantage Catheters due to reports of tip splits or separation, which may cause loss of function or complications.

    Product
    Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2324-2015·2015-08-12

    Medtronic Passive Biopsy Needle Kit Recalled for Adhesive Defect

    Medtronic is recalling 1,415 Passive Biopsy Needle Kits because compromised adhesive may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.

    Product
    Medtronic Passive Biopsy Needle Kit, Part Number 9733068 - Passive Biopsy Needle Kit. The image guided Passive Biopsy Needle is an accessory instrument with the StealthStation System. The Biopsy Needle is intended to be used for stereotaxy biopsy of brain tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide