The Recall Desk

State

Minnesota product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55351–55375 of 81678

  • ModerateFDA (Devices)·Z-1123-2016·2016-03-23

    Zimmer Manufacturing Recalls Distal Femoral Components for Sterility Concerns

    Zimmer Manufacturing B.V. is recalling specific distal femoral components used in total hip arthroplasty due to insufficient sealer calibration data.

    Product
    Product 25 consists of all product under product code: LPH and same usage: Item no: 234703104 DISTAL MEDIAL FEMORAL CON 234703206 DISTAL MEDIAL FEMORAL CON 234703208 DISTAL MEDIAL FEMORAL CON 234800504 DISTAL POSTERIOR/LATERAL 234800506 DISTAL POSTERIOR/LATERAL 234800508…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0773-2016·2016-03-23

    Teva Recalls Nabumetone Tablets Due to Missing Labels and Leaflets

    Teva Pharmaceuticals USA is recalling 576 bottles of Nabumetone 750 mg tablets because they lack required leaflets and approved labels.

    Product
    NABUMETONE Tablets USP, 750 mg, 100 count bottle,Teva Pharmaceutical Industries Ltd., Jerusalem, 91010, ISRAEL
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0778-2016·2016-03-23

    Pharmedium Recalls Subpotent Repinephrine Bitartrate Injection Bags

    Pharmedium Services, LLC is recalling specific lots of repinephrine bitartrate injection bags due to subpotency and discoloration confirmed by FDA analysis.

    Product
    NORepinephrine Bitartrate, 8 mg (32 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag Black, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-127-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·16V164000·2016-03-22

    Forest River Recalls 2016 Cherokee Grey Wolf Trailers for Placard Error

    Forest River is recalling 2016 Cherokee Grey Wolf recreational trailers because the Federal Placard lists incorrect tire and rim sizes, which may lead to overloading and tire blowouts.

    Product
    CHEROKEE — CHEROKEE GREY WOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V165000·2016-03-22

    Weiler Trucks Recalled for Missing Reflectors on LED Marker Lights

    Weiler is recalling 368 trucks from 2002-2016 because LED marker lights lack required reflectors, reducing visibility and increasing crash risk.

    Product
    WEILER — WEILER F3, F1, B3, B5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V161000·2016-03-21

    Winnebago Winnie Drop Recalled for Carbon Monoxide Leak Risk

    Winnebago is recalling 2016 Winnie Drop trailers because the refrigerator compartment may not seal properly, allowing carbon monoxide to enter the cabin.

    Product
    WINNEBAGO — WINNEBAGO WINNIE DROP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16126·2016-03-21

    Panasonic Recalls Lithium-ion Laptop Battery Packs Due to Fire Hazard

    Panasonic is recalling specific lithium-ion battery packs for CF-S10 Series laptops because a manufacturing defect poses a fire risk. No injuries have been reported.

    Product
    Lithium-ion Computer Battery Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·16125·2016-03-18

    RacerMate Recalls CompuTrainer Blue Flywheels Due to Shattering Risk

    RacerMate is recalling approximately 25,000 CompuTrainer Blue Flywheels because they can shatter during use, posing a risk of injury to riders and bystanders.

    Product
    CompuTrainer Blue Flywheels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V160000·2016-03-18

    GM Recalls 2014-2016 Chevrolet Caprice Police Pursuit for Steering Defect

    General Motors is recalling 2014-2016 Chevrolet Caprice Police Pursuit vehicles because corrosion may cause loss of electric power steering assist, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET CAPRICE POLICE PURSUIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16123·2016-03-18

    IKEA Recalls Gothem Floor and Table Lamps Due to Shock Hazard

    IKEA is recalling about 30,600 Gothem floor and table lamps because damaged cables can contact the metal body, posing a shock hazard. Consumers should stop using the lamps and return them for a full refund.

    Product
    Gothem floor and table lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E022000·2016-03-18

    ISS Recalls Evercraft Jack Stands Due to Potential Weld Defects

    International Specialty Services is recalling Evercraft jack stands sold by NAPA Auto Parts because improper welds may cause the stands to collapse, posing an injury risk.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V157000·2016-03-17

    Rosenbauer Commander Recall for Brake Pedal Piston Corrosion

    Rosenbauer is recalling 2012-2015 Commander vehicles because brake pedal pistons may corrode, making brakes difficult to activate or causing them to drag.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E021000·2016-03-17

    Battery-Biz Recalls Cyntur Lithium Ion Jumpstarters Due to Fire Risk

    Battery-Biz is recalling Cyntur CTJSLI Lithium Ion Jumpstarters because a faulty cable design may cause overheating and fire. Owners should contact customer service for a free replacement cable.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V158000·2016-03-17

    Jayco Recalls 2016 White Hawk Travel Trailers Due to Axle Defect

    Jayco is recalling 10 model year 2016 White Hawk travel trailers because they were built with axles rated for 3000 lbs instead of the required 3500 lbs, which may affect handling.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1063-2016·2016-03-16

    Arrow Percutaneous Insertion Tray Recalled for Potential Sheath Separation

    Arrow International is recalling Percutaneous Insertion Trays because the sheath body may separate from the hub, creating a potential for bleeding.

    Product
    Percutaneous Insertion Tray; Product Code: IAK-S7IT The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1058-2016·2016-03-16

    Arrow Ultra 8 IAB Recalled for Potential Sheath Separation and Bleeding Risk

    Arrow International is recalling Ultra 8 IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.

    Product
    Ultra 8 IAB: 8Fr 40cc; Product Code: IAB-05840-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0740-2016·2016-03-16

    R&D Technical Center Recalls Peanut Drop Coating for Listeria

    R&D Technical Center is recalling Clasen Quality Coatings NH Atlas 1M Creamy Peanut Drop after a positive Listeria monocytogenes test.

    Product
    Clasen Quality Coatings NH Atlas 1M Creamy Peanut Drop, Item # 12649, Net Wt. 50 lbs (22.68 KG)
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Devices)·Z-1059-2016·2016-03-16

    Arrow UltraFlex IAB Recall: Sheath Separation Risk

    Arrow International is recalling UltraFlex IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.

    Product
    UltraFlex IAB: 7.5Fr 30cc; Product Code: IAB-06830-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0733-2016·2016-03-16

    Living Tree Community Foods Recalls Organic Macadamia Nuts Due to Salmonella Risk

    Living Tree Community Foods is recalling 4 oz. pouches of Organic Macadamia Nuts due to potential Salmonella contamination. The recall affects 195 units distributed in 23 US states.

    Product
    Living Tree Community Foods Organic Macadamia Nuts, 4 oz. plastic pouch. Certified Organic
    Category
    Food
    Distribution
    23 states
  • CriticalFDA (Devices)·Z-1061-2016·2016-03-16

    Arrow RediGuard IAB Recall Due to Sheath Separation Risk

    Arrow International is recalling RediGuard IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.

    Product
    RediGuard IAB: 7Fr 30cc; Product Code: IAB-S730C The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0771-2016·2016-03-16

    Tf Supplements Recalls Rhino 7 3000 Due to Undeclared Ingredients

    Tf Supplements is recalling Rhino 7 3000 bottles because they contain undeclared desmethyl carbondenafil and dapoxetine and were marketed without an approved NDA or ANDA.

    Product
    RHINO 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0772-2016·2016-03-16

    Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients

    Tf Supplements is recalling Rhino 7 Platinum 3000 because it contains undeclared desmethyl carbondenafil and dapoxetine and was marketed without an approved NDA or ANDA.

    Product
    Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA, UPC 700729253748
    Category
    Drug
    Distribution
    Distributed nationwide