State

Minnesota product recalls

73,570 recalls have nationwide distribution and so reach Minnesota. 7,844 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,844
Critical: 1,139
Severe: 2,243
Most recent: 2026-10-24

Of the 7,844 recalls naming Minnesota we have scored against our rubric, 1,139 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,243 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,844 recalls whose distribution notice names Minnesota specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24351–24375 of 81414

ModerateFDA (Drugs)·D-0439-2022·2022-02-02
Drug Recall: Profound Dental Gel CGMP Deviations
Edge Pharma is voluntarily recalling 353 jars of Profound Dental Gel nationwide due to Current Good Manufacturing Practice (CGMP) deviations identified during the manufacturing process.
Product
Profound Dental Gel, Lidocaine HCl/Prilocaine HCl/Tetracaine HCl, 10%/10%/4% Raspberry Marshmallow, 30 grams per jar, Multiple Dose Container For Topical Oral Use,Edge Pharma LLC, 856 Hercules Dr. Colchester, VT 05446, NDC 05446-0790-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0452-2022·2022-02-02
Proctofoam Topical Aerosol Recalled for cGMP Manufacturing Deficiencies
Mylan Pharmaceuticals Inc is voluntarily recalling Proctofoam HC (hydrocortisone acetate 1% and pramoxine hydrochloride 1%) topical aerosol due to current Good Manufacturing Practice (cGMP) deficiencies. The recall affects 233,199 10-gram aerosol containers distributed nationwide.
Product
PROCTOFOAM — PROCTOFOAM (PRAMOXINE HYDROCHLORIDE HYDROCORTISONE ACETATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0409-2022·2022-02-02
Mitomycin-C Ophthalmic Solution Recall Due to Sterility Assurance
Edge Pharma is recalling Mitomycin-C sterile ophthalmic solution syringes because the manufacturer lacks assurance of sterility. The recall affects 154 syringes distributed nationwide.
Product
Mitomycin-C, Sterile Ophthalmic Solution, Preservative Free, 0.16mg/0.8mL (0.2 mg/mL), 0.8 mL per syringe, Single Use Syringe, For Topical Ophthalmic Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1011-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0457-2022·2022-02-02
CariFree CTx36 Kit recalled for subpotent fluoride content
Dental Alliance Holdings LLC is recalling the CTx36 Kit because it contains less sodium fluoride than stated on the product label. Affected patients should contact their dentist.
Product
CTx36 Kit, contains three tubes of CariFree CTx4 Gel 5000, 1.1% Neutral Sodium Fluoride Mint, 2 oz (57 g) Rx only NDC: 61578-205-01 Manufactured by Oral BioTech Albany, Oregon 97321 and six boxes of 4fl.oz. Carifree CTx4 Treatment Rinse.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0436-2022·2022-02-02
LT Topical Cream Recalled for Manufacturing Practice Deviations
Edge Pharma, LLC is recalling 74 jars of LT Topical Cream (Lidocaine/Tetracaine) nationwide due to deviations from Current Good Manufacturing Practice (CGMP). The firm initiated the voluntary recall on December 6, 2021.
Product
LT Topical Cream, Lidocaine/Tetracaine, 23%/7%, 60gm per jar, Multiple Dose Container for Topical Use, Edge Pharma, LLC, 856 Hercules, VT, Colchester, VT 05446, NDC 05446-1647-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0442-2022·2022-02-02
Profound-PE Dental Gel Recalled for Manufacturing Deviations
Edge Pharma, LLC is recalling Profound-PE Dental Gel nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects 175 jars of the topical oral anesthetic gel.
Product
Profound-PE Dental Gel, Lidocaine HCl/Prilocaine HCl/Tetracaine HCl/Phenylephrine, 10% / 10% / 4% / 2%, Spear-Peppermint, Multiple Dose Container for Topical Oral Use, 30 grams per jar, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT, 05446, NDC 05446-0408-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0519-2022·2022-02-02
GE Vscan Extend Ultrasound Device May Fail to Power On
GE Vscan Extend portable ultrasound devices may not power on due to battery depletion caused by improper device handling. The device must be properly turned off before removing the battery or disconnecting from power sources.
Product
GE Vscan Extend, being sold as "Vscan Extend Dual DICOM"
Category
Medical Device
Distribution
50 states
ModerateFDA (Drugs)·D-0458-2022·2022-02-02
CariFree CTx4 Gel 5000 Sample Boxes Recalled for Subpotent Fluoride
CariFree sample boxes containing CTx4 Gel 5000 are being recalled because the product contains less Sodium Fluoride than stated on the label. Affected lots are 492106 and 492107, distributed nationwide.
Product
CariFree sample boxes, contains one tube of CariFree CTx4 Gel 5000, 1.1% Neutral Sodium Fluoride Mint, 2 oz (57 g) Rx only NDC: 61578-205-01 Manufactured by Oral BioTech Albany, Oregon 97321.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0393-2022·2022-02-02
Metoprolol Succinate Extended-Release Tablets Recalled for Failed Dissolution
Ascend Laboratories is recalling Metoprolol Succinate Extended-Release Tablets 25 mg nationwide because the tablets failed to meet dissolution specifications, which may affect how the medication releases in the body.
Product
METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE ER TABLETS)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0453-2022·2022-02-02
CariFree CTx4 GEL 5000 Recalled for Subpotent Fluoride Content
CariFree CTx4 GEL 5000 (Lot 142017) contains less sodium fluoride than stated on the label. The product is being recalled and consumers should contact their healthcare provider with questions.
Product
CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint, 2 oz (57 g) Rx only NDC: 61578-205-01 Manufactured by Oral BioTech Albany, Oregon 97321 Distributed in 12-pk/cases
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V047000·2022-02-01
Seagrave Recalls 2021 Capitol and Marauder Vehicles for Axle Defect
Seagrave is recalling 2021 Capitol and Marauder vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake unexpectedly and increasing crash risk.
Product
SEAGRAVE — SEAGRAVE CAPITAL, MARAUDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V046000·2022-02-01
Jayco Pinnacle and North Point Trailers Recalled for Tire Belt Separation
Jayco is recalling 2021-2022 Pinnacle and North Point trailers with Sailun tires that may experience belt separation, potentially causing loss of vehicle control. Free tire replacement is available through dealers.
Product
JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL PINNACLE, NORTH POINT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V045000·2022-02-01
Tesla vehicles seatbelt warning chime may fail to activate
Tesla is recalling vehicles with seatbelt warning chimes that may not activate when the driver has not fastened their seat belt. The fix is a free over-the-air software update.
Product
TESLA — TESLA MODEL 3, MODEL Y, MODEL S, MODEL X
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22T002000·2022-02-01
Bridgestone Recalls Firestone Tires Due to Belt Separation Risk
Bridgestone is recalling specific Firestone Transforce tires because an incorrect inner liner compound could cause belt separation, increasing the risk of a crash.
Product
TIRES:TREAD/BELT recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V043000·2022-01-31
Newmar Recalls 2020-2022 Motor Homes Due to Tire Valve Stem Defect
Newmar is recalling 2020-2022 Super Star and Supreme Aire motor homes because a tire valve stem extension may be damaged, causing loss of tire pressure and increasing crash risk.
Product
NEWMAR — NEWMAR SUPREME AIRE, SUPER STAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22E005000·2022-01-28
Samsung SDI Recalls High Voltage Battery Packs for Sudden Power Loss
Samsung SDI is recalling specific high voltage battery packs that may fail, causing a sudden loss of drive power and increasing crash risk.
Product
ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V042000·2022-01-28
Mercedes-Benz Recalls 2021 AMG GT Black Series for Wiring Harness Defect
Mercedes-Benz is recalling 2021 AMG GT Black Series vehicles because an incorrectly sized front wheel speed sensor wiring harness may damage, impairing safety systems and increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG GT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V040000·2022-01-28
2021-2022 Porsche Cayenne Rear Axle Alignment Safety Recall
Porsche is recalling 2021-2022 Cayenne vehicles due to potential rear axle misalignment following prior repairs. The defect may cause premature tire wear and increase crash risk.
Product
PORSCHE — PORSCHE CAYENNE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V041000·2022-01-28
2022 Forest River Vengeance Trailers Recalled for Incorrect Tire Pressure Labels
Forest River is recalling certain 2022 Vengeance Fifth Wheel trailers because the tire pressure labels may display incorrect information for the front tires, which could result in under-inflated tires and increase the risk of a crash.
Product
FOREST RIVER — FOREST RIVER VENGEANCE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V038000·2022-01-28
2013-2021 Grand Design recreational vehicles recalled for fire hazard
Grand Design RVs (2013-2021) are recalled for an improperly secured 110-volt refrigerator wire that may cause electrical arcing and fire. Dealers will inspect and replace damaged wiring at no cost.
Product
GRAND DESIGN — GRAND DESIGN SOLITUDE, MOMENTUM, REFLECTION
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22718·2022-01-28
Matrix T1 and T3 Commercial Treadmills Recalled for Fire Hazard
Johnson Health Tech is recalling about 19,900 Matrix T1 and T3 Series commercial treadmills because the power cord can become loose from the power socket, causing sparking, smoking, melting, and fire. No injuries have been reported.
Product
Matrix T1 and T3 Series Commercial Treadmills
Category
Consumer Product
Distribution
Distributed nationwide
ModerateNHTSA·22V039000·2022-01-28
2020-2021 Grand Design Imagine Trailers Recalled for Sharp Cabinet Handles
Grand Design is recalling 2020-2021 Imagine travel trailers with cast aluminum cabinet handles that may have sharp edges. The sharp edges could cut or scrape occupants, and dealers will replace the handles free of charge.
Product
GRAND DESIGN — GRAND DESIGN IMAGINE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22E004000·2022-01-27
Prevost Recalls Seat Brackets That May Fail in Crashes
Prevost is recalling certain seat brackets that may not meet strength requirements, increasing injury risk in a crash.
Product
SEATS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V037000·2022-01-27
Tesla Vehicles: Full Self-Driving Software May Skip Required Stops
Tesla is recalling certain 2016-2022 Model S and X, 2017-2022 Model 3, and 2020-2022 Model Y vehicles. The Full Self-Driving (Beta) software rolling stop feature may allow vehicles to pass through all-way stop intersections without stopping, increasing crash risk.
Product
TESLA — TESLA MODEL S, MODEL X, MODEL 3, MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V035000·2022-01-27
RAM 2500-5500 Recall for Windshield Wiper Arm Loosening
Chrysler is recalling 2019-2020 RAM 2500-5500 vehicles because wiper arms may loosen, reducing visibility in certain weather conditions.
Product
RAM — RAM 2500, 4500, 3500, 5500
Category
Vehicle
Distribution
Distributed nationwide