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.

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.

48401–48425 of 81668

  • SevereFDA (Drugs)·D-0682-2017·2017-05-03

    Isomeric Pharmacy Recalls Methylprednisolone Acetate Injection Vials for Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 2,352 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.

    Product
    Methylprednisolone Acetate 80 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1011, barcode 3 70285 10111 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1538-2017·2017-05-03

    Heartware Recalls HVAD System Controllers for Exchange

    Heartware is recalling all HVAD System Controllers currently on the market to exchange them for the next generation HVAD Controller (Controller 2.0).

    Product
    HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HeartWare Ventricular Assist System…
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Food)·F-1893-2017·2017-05-03

    Pepper Colby-Jack Cheese Recalled for Potential Listeria Contamination

    Deutsch Kase Haus, LLC is recalling various brands of pepper cheese due to potential Listeria monocytogenes contamination. The product was distributed across 11 states.

    Product
    Pepper Colby-Jack (or: Pepper Marble Jack; Lightning Jack; Thunder Jack; Firecracker; Jalapeno Jack; Jumping Jack) cheese. All affected product private labeled for other companies. Brands: Guggisberg; Dutch Farms; Amish Classics; Lipari Old Tyme; Walnut Creek…
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-0686-2017·2017-05-03

    Isomeric Pharmacy Recalls Testosterone Injection Vials Due to Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 2,156 vials of Testosterone Cypionate and Propionate injection due to production processes that cannot assure sterility.

    Product
    Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1200, barcode 3 70285 12003 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V298000·2017-05-03

    Audi Recalls Q5 and Q7 Models for Fuel Pump Flange Crack Risk

    Volkswagen Group of America is recalling 2013-2017 Audi Q5 and Q7 vehicles because a fuel pump flange may crack, allowing fuel to leak and increasing fire risk.

    Product
    AUDI — AUDI Q5, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0685-2017·2017-05-03

    Isomeric Pharmacy Recalls Injection Vials Due to Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 851 vials of a multi-dose injection product because production processes cannot assure sterility.

    Product
    Cyanocobalamin 1 mg/mL/ Methionine 25 mg/mL/ Inositol 50 mg/mL/ Choline 50 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1101, barcode 3 70285 11013 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0681-2017·2017-05-03

    Isomeric Pharmacy Recalls Methylprednisolone Acetate Injection Vials for Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 4,001 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.

    Product
    Methylprednisolone Acetate 40 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1010, barcode 3 70285 10101 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2095-2017·2017-05-03

    ConAgra Recalls Premium Hunt's Chili Kits for Potential Salmonella

    ConAgra Foods is recalling Premium Hunt's Chili Kits due to potential Salmonella contamination in the spice packets. The recall covers 5,458 cases distributed nationwide.

    Product
    Premium Hunt's Chili Kit, Total NET WT 44.8 OZ (2.80 LB) 1.27kg; Directions: 1) Cook and stir meat in saucepan over medium-high 7 minutes or until done; drain. 2) Stir in all remaining ingredients; simmer 10 minutes, stirring occasionally. Con Agra Foods, P.O BOX 3768, Dept.…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1888-2017·2017-05-03

    Remel Blood Agar Plates Recalled for Listeria Contamination

    Remel Inc is recalling Blood Agar plates due to confirmed surface contamination with Listeria monocytogenes. The products were distributed nationwide and in Puerto Rico.

    Product
    Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood Agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1877-2017·2017-05-03

    Cardiovascular Systems Recalls ViperWire Advance Guide Wires Due to Packaging Error

    Cardiovascular Systems Inc is recalling 595 units of ViperWire Advance guide wires because 0.018-inch products were packaged as 0.014-inch.

    Product
    ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14. Product Usage: The Stealth 360 Orbital PAD System and the Diamondback 360 Peripheral Orbital Atherectomy System are percutaneous orbital atherectomy systems…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1878-2017·2017-05-03

    Ulrich Medical Recalls uNion Cervical Plate System for Screw Mechanism Defect

    Ulrich Medical USA Inc is recalling 4,854 uNion Cervical Plate Systems because static plate screws may disassociate. The recall covers devices distributed in 20 US states.

    Product
    uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the cervical spine (C2 to Ti). The system is to be used to provide stabilization of the anterior cervical spine as an adjunct to fusion for the treatment of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0684-2017·2017-05-03

    Isomeric Pharmacy Recalls Triamcinolone Diacetate Vials Due to Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 1,951 vials of Triamcinolone Diacetate injection because production processes cannot assure sterility. The FDA has classified this as a Class II recall.

    Product
    Triamcinolone Diacetate 40 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1021, barcode 3 70285 10211 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1889-2017·2017-05-03

    Merit Medical Recalls 1 mL Medallion Syringes Due to Plunger Tip Defect

    Merit Medical Systems is voluntarily recalling 1 mL Medallion Syringes because of a defect in the syringe plunger tip.

    Product
    1 mL Medallion¿ Syringe. Catalog Numbers: 701989001, K01-05197P, MSS011-YP, K01-07946P, MSS011, MSS011-LB, MSS011-R, MSS011-Y, MSS011P, MSS011-LBP, MSS011-DG, K08-02926AP, K01-07742P, K10-05457P.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1884-2017·2017-05-03

    XTANT Medical Recalls 5.5mm CoCr Straight Rods Due to Labeling Error

    XTANT Medical Inc. is recalling 97 units of 5.5mm CoCr Straight Rods because the labels may incorrectly identify the material as Ti6Al-4V ELI instead of Cobalt Chromium.

    Product
    5.5mm Diameter x 500mm CoCr Straight Rod, Model number X077-0420. The product is packaged in plastic bags with one piece per bag. Product Usage: The 5.5mm dia. X 500 mm CoCr Straight Rod is an accessory to the Fortex Pedicle Screw System. It is a straight rod connected…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1875-2017·2017-05-03

    Siemens ACUSON S Family Ultrasound Systems Recalled for Image Display Defects

    Siemens is recalling 2,045 ACUSON S Family ultrasound systems because the 18L6 HD transducer may display a triple image or a dark band, potentially affecting diagnostic accuracy.

    Product
    18L6 HD transducer on the ACUSON S Family ultrasound systems with software versions VD10A or VD10C; Model numbers: 18L6 HD transducer  10041227 & 10789400 S1000  10441701 S2000  10041461 S2000 (Refurb) - 10440017 S3000  10441730 Radiology: The ultrasound imaging…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1881-2017·2017-05-03

    Zimmer CAS Recalls Navitrack Knee Software Due to Calibration Crash

    Zimmer CAS is recalling Navitrack System - OS Knee Universal software due to a calibration sequence crash. The recall affects 105 units distributed worldwide.

    Product
    Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in the placement of total knee replacement components
    Category
    Medical Device
    Distribution
    21 states
  • LowFDA (Drugs)·D-0678-2017·2017-05-03

    Novartis Recalls Isopto Carpine Eye Drops for Impurity Failures

    Novartis Pharmaceuticals is recalling specific lots of Isopto Carpine eye drops due to failed impurities and degradation specifications.

    Product
    Isopto Carpine (pilocarpine hydrochloride opthalmic solution) 4%, packaged in 15 mL bottle, Rx only, Manufactured by: Alcon Laboratories, Inc. Fort Worth Texas 76134 USA NDC 0998-0206-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1876-2017·2017-05-03

    Becton Dickinson Recalls Trypticase Soy Agar and Chocolate Agar I-Plates

    Becton Dickinson is recalling one lot of Trypticase Soy Agar and Chocolate Agar I-Plates because they may fail to recover specific Haemophilus organisms.

    Product
    BBL Trypticase Soy Agar with 5% Sheep Blood (TSA II) and Chocolate II Agar (GC II Agar with Hemoglobin and IsoVitaleX)  I Plate Product Usage: Testing - Trypticase Soy Agar with 5% Sheep Blood is used for the growth of fastidious organisms and for the visualization of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V292000·2017-05-02

    Forest River Recalls 2014 XLR Toyhaulers Due to Axle Bolt Issue

    Forest River is recalling 2014 XLR Hyperlite toyhaulers because an axle bolt may not be properly seated, which could cause the axle to shift and lead to a loss of vehicle control.

    Product
    FOREST RIVER — FOREST RIVER XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V299000·2017-05-02

    Prevost Recalls Motor Coaches Due to Trailer Hitch Fastener Loosening Risk

    Prevost is recalling 2014-2017 motor coaches because trailer hitch fasteners may loosen, potentially causing the hitch to detach and increasing crash risk.

    Product
    PREVOST — PREVOST X3-45, H3-45, H3-45 VIP, X3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17145·2017-05-02

    Goodman Recalls Gas Furnaces Due to Electrical Shock Hazard

    Goodman is recalling about 4,100 gas-fired furnaces because the blower motor is not grounded, posing an electrical shock hazard to individuals servicing the units.

    Product
    Gas-fired furnaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide