The Recall Desk

State

Minnesota product recalls

73,817 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.

Which agencies issued them

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45751–45775 of 81668

  • ModerateFDA (Devices)·Z-3125-2017·2017-09-20

    Leica Biosystems Recalls PAX8 Antibody Due to Temperature Deviation

    Leica Biosystems Richmond Inc. is recalling five units of PAX8 antibody because a transit delay may have caused the product to be stored outside required temperature limits.

    Product
    Cell Marque, PAX8 (MRQ-50 Mab.), 7 mL, REF PA0808, IVD, This antibody is intended for in vitro diagnostic (IVD) use. PAX-8 (MRQ-50) Mouse Monoclonal Primary Antibody is intended for laboratory use in the detection of the PAX-8 protein in formalin-fixed, paraffin-embedded tissue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1138-2017·2017-09-20

    Medline Recalls Mislabelled Vitamin A&D Ointment Packets

    Medline Industries is recalling Vitamin A&D Ointment packets that are incorrectly labeled as petroleum jelly. The outer boxes are correctly labeled.

    Product
    Vitamin A&D Ointment (petroleum 93.5%), Skin Protectant, NET Wt. 0.18 OZ (5g), Manufactured for Medline Industries, Inc., Northfield, IL 60093 USA. NDC: 53329-090-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3129-2017·2017-09-20

    Fujifilm Endoscope Corrective Action Following FDA Inspection

    Fujifilm Medical Systems U.S.A., Inc. is conducting a corrective action for specific endoscope models following an FDA inspection.

    Product
    Fujifilm Endoscope Models ED-250XL5 ED-250XT5 ED-450XT5 ED-450XL5 Product Usage: This product is a medical endoscope for the duodenum and upper GI tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach and duodenum. This…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3123-2017·2017-09-20

    Leica Biosystems Recalls MSH6 Antibody Due to Temperature Deviation

    Leica Biosystems Richmond Inc. is recalling 13 units of MSH6 antibody (REF PA0804) because a delay in transit may have caused the product to be stored outside of required temperature ranges.

    Product
    Cell Marque, MSH6 (44 Mab.), 7 mL, REF PA0804, IVD, The antibody is intended for in vitro diagnostic (IVD) use. MSH6 is a mismatch repair gene which is deficient in a high proportion of patients with microsatellite instability (MSI-H). This finding is associated with the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1139-2017·2017-09-20

    VistaPharm Recalls Hydrocodone and Acetaminophen Oral Solution Due to Labeling Error

    VistaPharm, Inc. is recalling 3,084 bottles of Hydrocodone Bitartrate and Acetaminophen Oral Solution because the product was incorrectly labeled as a Class III controlled substance instead of a Class II controlled substance.

    Product
    Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL (Cherry Flavored), 473 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771 ---- NDC 66689-023-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3128-2017·2017-09-20

    Fujifilm ED-530XT Endoscope Manuals Recalled Following FDA Inspection

    Fujifilm is recalling 260 user manuals for the ED-530XT endoscope following an FDA inspection. The recall is a corrective action to address documentation issues.

    Product
    Fujifilm Endoscope Model ED-530XT Product Usage: This product is a medical endoscope for the duodenum and upper GI tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach and duodenum. This product is not used for any other…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V574000·2017-09-19

    Mercedes-Benz Recalls Four 2017 Models for Steering Defect

    Mercedes-Benz is recalling four 2017 vehicles due to improperly welded steering pins that may disable power assist, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300, AMG E43, GLC300, AMG C43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E051000·2017-09-17

    Curt Trailer Hitches Recalled for Mini Clubman and Countryman Models

    Curt Manufacturing is recalling Class 1 trailer hitches for 2016-2018 Mini Clubman and Countryman vehicles because the mounting points may be inadequate, causing the hitch to sag or separate.

    Product
    MINI — MINI COUNTRYMAN, CLUBMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V571000·2017-09-15

    Nissan Recalls 2017 Infiniti Q50 Vehicles for Air Bag Inflator Defect

    Nissan is recalling 2017 Infiniti Q50 and Q50 Hybrid vehicles because the driver's air bag inflator may be improperly welded, increasing injury risk in a crash.

    Product
    INFINITI — INFINITI Q50 HYBRID, Q50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·101-2017·2017-09-15

    Sausage Products Recalled for Undeclared Milk Allergen and Misbranding

    America New York RI Wang Food Group is recalling pork sausage products containing undeclared milk. The recall covers approximately 53,973 pounds distributed in New Jersey and New York.

    Product
    America New York RI Wang Food Group Recalls Sausage Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V573000·2017-09-15

    Forest River Recalls Vibe and Rainier Trailers for Propane Line Defect

    Forest River is recalling 2015-2018 Vibe and 2016-2018 Rainier recreational trailers because the liquid propane line may have insufficient clearance, posing a fire risk.

    Product
    FOREST RIVER — FOREST RIVER VIBE, RAINIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17224·2017-09-14

    Southwire Recalls Moonrays Globe Stake Lights Due to Fire Hazard

    Southwire is recalling Moonrays mystic globe and snow globe stake lights because light refraction can singe or melt nearby items, posing a fire hazard.

    Product
    Moonrays mystic globe and snow globe stake lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V569000·2017-09-14

    Mitsubishi Recalls Lancer Vehicles Due to Air Bag Inflator Rupture Risk

    Mitsubishi is recalling 2004-2006 Lancer and 2004 Lancer Sportback vehicles because the passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.

    Product
    MITSUBISHI — MITSUBISHI LANCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17C003000·2017-09-14

    Diono Recalls Multiple Convertible and Booster Car Seats for Crash Protection Defect

    Diono is recalling specific Radian, Olympia, Pacifica, and Rainier car seats manufactured between late 2013 and early 2017. The seats may not adequately protect children from chest injuries in crashes if installed forward-facing with only a lap belt.

    Product
    CHILD SEAT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V570000·2017-09-14

    Pierce Recalls 2015-2016 Vehicles for Steering Tie Rod Torque Defect

    Pierce Manufacturing is recalling 2015-2016 Arrow XT, Enforcer, Impel, Quantum, Saber, and Velocity vehicles because a steering axle nut may not be properly torqued, risking loss of steering.

    Product
    PIERCE — PIERCE IMPEL, ARROW XT, ENFORCER, SABER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V565000·2017-09-14

    Kimble Mixer Recalls 2014 Custom Chassis for Drive Axle Defect

    Kimble Mixer is recalling one 2014 Mixer Custom Chassis because improperly torqued hex nuts on the drive axle could cause the driveshaft to disconnect, increasing crash risk.

    Product
    KIMBLE — KIMBLE MIXER CUSTOM CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V567000·2017-09-14

    GM Recalls 2017-2018 Silverado and Sierra Trucks for Seat Belt Defect

    General Motors is recalling 2017-2018 Chevrolet Silverado and GMC Sierra trucks because front seat belt retractors may not perform correctly in a crash.

    Product
    GMC — GMC, CHEVROLET SIERRA 3500, SIERRA 2500, SILVERADO 3500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3538-2017·2017-09-13

    Shore Lunch Fish Breading Batter Mix Recalled for Salmonella Risk

    Southeastern Mills is recalling Shore Lunch Fish Breading Batter Mix because raw buttermilk solids may be contaminated with Salmonella.

    Product
    Shore Lunch, Fish Breading Batter Mix, Original Breading, Net Wt. 3.5 lbs. (1587g) and12/255 G (Canada).
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-3537-2017·2017-09-13

    Southeastern Mills Cheddar Garlic Biscuit Mix Recalled for Salmonella Risk

    Southeastern Mills is recalling Easy Drop Cheddar Garlic Drop Biscuit Mix because raw buttermilk solids may be contaminated with Salmonella.

    Product
    Southeastern Mills, Easy Drop Cheddar Garlic Drop Biscuit Mix, Net Wt. 7oz (198g).
    Category
    Food
    Distribution
    34 states
  • SevereNHTSA·17V566000·2017-09-13

    AEV Traumahawk Ambulances Recalled for Door Striker Bolt Failure

    Halcore Group is recalling 2016-2017 AEV Traumahawk ambulances because door striker bolts may fail under load, potentially allowing doors to open in a crash.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide