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.

Which agencies issued them

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.

58651–58675 of 81684

  • ModerateFDA (Devices)·Z-2376-2015·2015-08-19

    Biotronik Recalls Unapproved Pacemaker Programmer Software Versions

    Biotronik is recalling specific pacemaker programmer software versions because they are not approved for use in the United States.

    Product
    PSW 1203.U/1, PSW 1301.U, PSW 1307.U, PSW 1403.U, and PSW 1501.U Pacemaker Programmer software. Software approved for use with BIOTRONIK device programmers (trade names: Renamic and ICS 3000). Allows physicians to program devices to pace exclusively in the left ventricle.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1320-2015·2015-08-19

    Biotene PBF Toothpaste Recalled for Wood Fragments

    GlaxoSmithKline is recalling Biotene PBF toothpaste because wood fragments were found when the product was extruded.

    Product
    biotene PBF Toothpaste (Plaque-Biofilm Loosening Formula), a) 4.3 oz. (121.9 g) tubes, (NDC 0135-0559-01), biotene¿ PBF Paste, b) 4.5 oz.(127.6 g) tubes, (NDC 0135-0490-02), Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1324-2015·2015-08-19

    Sensodyne Toothpaste Recalled Due to Wood Fragments

    GlaxoSmithKline is recalling 325,504 tubes of Sensodyne toothpaste because wood fragments were found when the product was extruded.

    Product
    SENSODYNE — SENSODYNE (STANNOUS FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1317-2015·2015-08-19

    Biotene Gentle Mint Gel Recalled for Wood Fragments

    GlaxoSmithKline is recalling Biotene Gentle Mint Gel tubes because wood fragments were found in the product. Consumers should stop using the affected lots.

    Product
    biotene Gentle Mint Gel, 4.5 oz.(127.6 g) tubes, Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108, NDC 0135-0488-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2363-2015·2015-08-19

    Stryker Recalls Mispackaged Orthopedic Shoulder Trial Instruments

    Stryker is recalling 21 units of a shoulder trial instrument because the package contained the wrong part number.

    Product
    ReUnion TSA Shoulder System, Standard SR Humeral Head Trial, 48X18, Catalog number 5901-S-4818. Orthopedic manual surgical instrument. Howmedica Osteonics Corp. A Subsidiary of Stryker Corp. Stryker France Non-sterile Made in Cork Ireland
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2361-2015·2015-08-19

    Abbott Recalls i-Stat PT/INR Cartridges Due to Test Delays

    Abbott Point Of Care Inc. is recalling specific lots of i-Stat PT/INR Cartridges because they may generate excessive star outs, potentially delaying patient results.

    Product
    i-Stat PT/INR Cartridges List number 03P89-24 The cartridges are packaged in sealed pouches, one per pouch. There are 24 cartridges packed in a box. a prothrombin time test useful in monitoring patients receiving oral anticoagulation therapy such as coumadin or warfarin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1323-2015·2015-08-19

    Sensodyne Toothpaste Recalled Due to Wood Fragments

    GlaxoSmithKline is recalling Sensodyne toothpaste tubes because wood fragments were found in the product. Consumers should stop using the affected tubes.

    Product
    SENSODYNE — SENSODYNE (STANNOUS FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1318-2015·2015-08-19

    Biotene Fluoride Toothpaste Recalled for Wood Fragments

    GlaxoSmithKline is recalling Biotene fluoride toothpaste because wood fragments were found in the product. Consumers should stop using the affected tubes.

    Product
    BIOTENE — BIOTENE (SODIUM FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2360-2015·2015-08-19

    Stryker Recalls Mislabelled Triathlon Tibial Inserts for Knee Replacement

    Stryker Howmedica Osteonics is recalling 26 Triathlon tibial inserts because one unit was found in a package labeled for a different catalog number.

    Product
    Triathlon PS X3 Tibial Insert; No. 3 Triathlon TS Plus Tibial Insert X3 Poly 19 mm Product Usage: The Triathlon PS X3 (posterior stabilized), cat no 5532-G-xxx and X3 TS (total stabilizing) Plus, cat. no. 5537-G-XXX, Tibial Inserts are used in TKA surgeries. During surgery…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2951-2015·2015-08-19

    Mason Vitamins Recalls Mislabeled Coenzyme Q-10 50 mg Softgels

    Mason Vitamins, Inc. is recalling 13,027 bottles of Coenzyme Q-10 50 mg softgels because some bottles were mislabeled with the wrong dosage.

    Product
    Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes ENERGY in all Body Cells***Dietary Supplement 30 SOFTGELS***."
    Category
    Food
    Distribution
    31 states
  • SevereNHTSA·15V527000·2015-08-18

    Starcraft Transit Bus Recall for Fire Risk from Wiring

    Forest River is recalling 32 Starcraft transit buses due to an improperly routed cable that may cause an electrical short and fire.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALL STAR XL, XLT, ALL STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V529000·2015-08-18

    E-One Emergency Vehicles Recalled for Lighting and Siren Safety Defect

    E-One is recalling 2013-2016 Pumpers, Tankers, and Rescue vehicles because the master power switch does not link to the start circuit, allowing operation without lights or sirens.

    Product
    E-ONE — E-ONE RESCUE, TANKER, PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15218·2015-08-18

    Rite Aid Recalls Outdoor Dining Sets Due to Fall Hazard

    Rite Aid is recalling about 13,000 outdoor dining sets because chair arms and legs can bend, causing users to fall and potentially be injured.

    Product
    Outdoor Dining Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V528000·2015-08-18

    Mack Granite Trucks Recalled for Air Brake Reservoir Volume Defect

    Mack is recalling 2011-2016 Granite trucks because an air brake reservoir may have insufficient volume, potentially affecting braking performance and increasing crash risk.

    Product
    MACK — MACK GRANITE (GU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V526000·2015-08-18

    Turtle Top Transit Buses Recalled for Back-Up Camera Image Reversal

    Turtle Top is recalling certain 2014-2015 transit buses because the back-up camera system may display reversed images, increasing the risk of a crash.

    Product
    TURTLE TOP — TURTLE TOP VANTERRA, ODYSSEY, ODYSSEY XLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V525000·2015-08-18

    Starcraft Transit Buses Recalled for Potential Fuel Injector Failure

    Forest River is recalling 2013-2014 Starcraft All Star XL and 2013 XLT transit buses because fuel injectors may fail, potentially causing engine stalls and increasing crash risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALL STAR XL, XLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15219·2015-08-18

    Merck Recalls Temodar and Temozolomide Bottles with Cracked Caps

    Merck is recalling approximately 276,000 bottles of Temodar and Temozolomide capsules because cracked caps may fail to keep young children from accessing the medication.

    Product
    Bottles with cracked caps containing Temodar® (Temozolomide) and Temozolomide (generic) capsules
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V523000·2015-08-17

    Volvo Recalls 2012-2016 VAH Trucks for Steering Drag Link Defect

    Volvo is recalling 2012-2016 VAH trucks because a damaged steering component may corrode, potentially causing loss of steering and increasing crash risk.

    Product
    VOLVO — VOLVO VAH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V521000·2015-08-17

    Mack Pinnacle Trucks Recalled for Brake Chamber Mounting Defect

    Mack is recalling 2013-2015 Pinnacle trucks because incorrectly mounted brake chambers may contaminate calipers, increasing stopping distance and crash risk.

    Product
    MACK — MACK PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V524000·2015-08-17

    Volvo Recalls 2012-2015 VNL and VNM Trucks for Brake Handle Defect

    Volvo is recalling 2012-2015 VNL and VNM trucks because the trailer hand brake handle may not return to the off position, potentially causing wheel overheating, fire, or tire blowout.

    Product
    VOLVO — VOLVO VNM, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V522000·2015-08-17

    Mack Trucks Recall Chassis Harness and Air Line Clipping Defect

    Mack Trucks is recalling specific model year 2009-2016 Granite, Titan, and Pinnacle trucks because chassis harness and air lines may not be properly clipped, risking driveline entanglement.

    Product
    MACK — MACK GRANITE (GU), TITAN, PINNACLE (CHU)
    Category
    Vehicle
    Distribution
    Distributed nationwide