The Recall Desk

State

Minnesota product recalls

73,718 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,849
Critical
1,137
Severe
2,245
Most recent
2026-10-28

Of the 7,849 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 2,245 (29%) are Severe.

These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28076–28100 of 81567

  • SevereFDA (Devices)·Z-1309-2021·2021-04-07

    CareFusion Recalls BD Alaris Infusion Pump Keypads Due to Fluid Ingress

    CareFusion is recalling BD Alaris Infusion Pump Module Keypads and Door Assembly Kits because fluid ingress can cause unresponsive or stuck keys, potentially delaying medication infusion.

    Product
    BD Alaris Infusion Pump Module Model 8100 Pump Module Keypad; and Pump Module Door Assembly Replacement Kit with Pump Module Keypad, Parts: 49000239; 49000346; 49000438; 49000439.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0315-2021·2021-04-07

    Zydus Recalls Acyclovir Sodium Injection Due to Crystallization

    Zydus Pharmaceuticals is recalling Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.

    Product
    ACYCLOVIR — ACYCLOVIR (ACYCLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V244000·2021-04-07

    New Flyer Recalls Electric Buses Due to Inverter Firmware Errors

    New Flyer is recalling certain 2013-2021 electric buses because firmware errors in the inverters may cause the electric drive system to shut down, increasing the risk of a crash.

    Product
    NEW FLYER — NEW FLYER XE60, XE35, XE40, XHE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1313-2021·2021-04-07

    Medtronic Bio-Console 560 Blood Pumping Console Recalled for Electrical Failure

    Medtronic is recalling Bio-Console 560 devices because an electrical component may fail, causing the pump to stop and potentially producing smoke or a burning odor.

    Product
    Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console, Model Numbers: 560BC, 560BC1, 560BCS, 560BCS1, R560BCS1. Used in cardiopulmonary bypass (CPB) procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V243000·2021-04-07

    Utility Trailer Recalls VS2DC, VS2DX, VS3DX Models for Missing Weld

    Utility Trailer is recalling 2006-2021 VS2DC, VS2DX, and VS3DX trailers because a missing weld may cause the slider rail to detach, increasing crash risk.

    Product
    UTILITY TRAILER — UTILITY TRAILER VS3DX, VS2DX, VS2DC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1330-2021·2021-04-07

    Siemens ACUSON Sequoia Ultrasound Systems Recalled for Incorrect Delivery Date Calculations

    Siemens is recalling 1,172 ACUSON Sequoia ultrasound systems because a software error may calculate incorrect Estimated Dates of Delivery, potentially influencing clinical decisions.

    Product
    Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Food)·F-0369-2021·2021-04-07

    Caribou Coffee Turkey Sandwich Recalled for Listeria Contamination Risk

    J & J Distributing Company is recalling Caribou Coffee Turkey Sandwiches due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in eight states.

    Product
    Caribou Coffee Turkey Sandwich, Net Wt. 9.0oz. (255g)
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1323-2021·2021-04-07

    Nuvasive PRECICE STRYDE Intramedullary Nail Recall for Biological Safety Concerns

    Nuvasive Specialized Orthopedics is recalling PRECICE STRYDE intramedullary nails due to complaints of adverse events potentially related to biological safety, including pain and bony abnormalities.

    Product
    PRECICE STRYDE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21103·2021-04-07

    Epicure Recalls Glass Prep Bowls Due to Laceration Hazard

    Epicure is recalling glass prep bowls that may shatter during use, posing a laceration hazard. Consumers should stop using the product and contact Epicure for a free replacement.

    Product
    Epicure Prep Bowls (Set of Four)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0317-2021·2021-04-07

    Ferring Recalls ZOMA-Jet 5 Demonstration Kits Due to Defective Delivery System

    Ferring Pharmaceuticals is recalling 301 ZOMA-Jet 5 Demonstration Kits because the injector pen may break apart and disintegrate into pieces.

    Product
    ZOMA-Jet 5 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 5mg vial, Rx only, ZOMA-Jet 5 Demonstration Kit contains -ZOMA-Jet 5 device - 5 Needle-Free Head A's - 2 Vial Adaptors - 1 Carrying Case - 1 User Manual; Manufactured for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0371-2021·2021-04-07

    Earthgrown Mini Taco Dip Recalled for Listeria Contamination Risk

    J & J Distributing Company is recalling Earthgrown Mini Taco Dip due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in eight states.

    Product
    Earthgrown Mini Taco Dip, Net Wt. 8oz. (227g), UPC 6 10014 22341 0, Packed By J&J Distributing Inc. 653 Rice St, St Paul, MN 55103
    Category
    Food
    Distribution
    8 states
  • HighCPSC·21102·2021-04-07

    RH Recalls Children's Bath Wraps for Flammability Standard Violations

    RH is recalling approximately 55,700 children's bath wraps in the U.S. because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.

    Product
    Animal, Heathered Plush and Luxe Sherpa Children's Bath Wraps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0375-2021·2021-04-07

    J & J Distributing Recalls Taco Dip for Listeria Risk

    J & J Distributing Company is recalling 8-ounce Kwik Trip Taco Dip due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in eight states.

    Product
    Taco Dip [Kwik Trip], Net Wt. 8oz (227g), UPC 0 38232 36091 3, Distributed By H. Brooks & Co. Mpls MN 55112
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0372-2021·2021-04-07

    Haug Fresh Mini 7 Layer Dip Tray Recalled for Listeria Risk

    J & J Distributing Company is recalling Haug Fresh Mini 7 Layer Dip Trays due to potential Listeria monocytogenes contamination.

    Product
    Haug Fresh Mini 7 Layer Dip Tray, Net Wt. 22oz (624g), UPC 6 10014 16414 0, Packed and Distributed by J&J Distributing, St Paul Mn 55103
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1324-2021·2021-04-07

    Nuvasive Precice Bone Transport Nail Recalled for Biological Safety Concerns

    Nuvasive Specialized Orthopedics is recalling 226 Precice Bone Transport nails due to complaints of pain and bony abnormalities related to biological safety.

    Product
    Precice Bone Transport - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0373-2021·2021-04-07

    Fresh Thyme Taco Dip Recalled for Listeria Contamination

    Fresh Thyme Taco Dip (10oz) is recalled due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in 8 states.

    Product
    Fresh Thyme Taco Dip, Net Wt. 10oz (283g), UPC 8 41330 12368 3
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1328-2021·2021-04-07

    Alcon Custom Ophthalmic Surgical Procedure Packs Recalled for Mold

    Alcon is recalling 249,853 custom ophthalmic surgical procedure packs because mold was found on gowns included in the packages.

    Product
    Alcon Custom Ophthalmic Surgical Procedure Packs
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0370-2021·2021-04-07

    Tastebuds Taco Platter Recalled for Listeria monocytogenes Contamination Risk

    J & J Distributing Company is recalling Tastebuds Taco Platters due to potential Listeria monocytogenes contamination. The product was distributed to retail locations in eight states.

    Product
    tastebuds Taco Platter, Net Wt. 26oz. (738g), UPC 0 38232 31683 5; Net Wt. 15.8oz (448g), UPC 0 38232 33235 4, Distributed By H. Brooks & Co Mpls MN 55112
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1342-2021·2021-04-07

    Diasorin Recalls LIAISON 1-84 PTH Assay Due to Falsely Elevated Results

    Diasorin Inc. is recalling LIAISON 1-84 PTH Assay kits because the system may produce falsely elevated parathyroid hormone results.

    Product
    LIAISON 1-84 PTH Assay - Product Usage: is an in vitro chemiluminescent immunoassay (CLIA) intended for the quantitative determination of parathyroid hormone (1-84) in human serum and EDTA plasma. Measurements of parathyroid hormone levels are used in the differential diagnosis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0374-2021·2021-04-07

    J & J Distributing Recalls Tastebuds Taco Dip for Listeria Risk

    J & J Distributing Company is recalling 371 units of Tastebuds Taco Dip due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in eight states.

    Product
    tastebuds Taco Dip, Net Wt. 9oz (255g), UPC 0 38232 31612 5, Distributed By H. Brooks & Co Mpls MN 55112
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1325-2021·2021-04-07

    Nuvasive Recalls PRECICE Plates Due to Biological Safety Concerns

    Nuvasive Specialized Orthopedics Inc is recalling 40 PRECICE Plate units worldwide due to complaints of adverse events potentially related to biological safety.

    Product
    PRECICE PLATE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1333-2021·2021-04-07

    Biocare Medical IntelliPath FLX Automated Staining Instrument Recall

    Biocare Medical is recalling 72 IntelliPath FLX instruments due to a software defect that may cause random movement and buffer dispensing errors.

    Product
    BIOCARE Medical , IntelliPath FLX, Automated Staining Instrument, Ref: " Model Number:IPS0001US and IPS0001INTL containing software version 3.5.3.1
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Food)·F-0368-2021·2021-04-07

    J & J Distributing Recalls Taco Platter Due to Listeria Risk

    J & J Distributing Company is recalling Taco Platters sold at Kwik Trip locations due to potential Listeria monocytogenes contamination.

    Product
    Taco Platter [Kwik Trip], Net Wt. 15.8oz (448g), UPC 0 38232 36090 6, Distributed By H. Brooks & Co. Mpls MN 55112
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1311-2021·2021-04-07

    Hollister Recalls Vertical Drain Tube Attachment Devices Due to Separation Risk

    Hollister Incorporated is recalling Vertical Drain Tube Attachment Devices (VTAD) because the tube holder can separate from the securing barrier, risking tube migration or loss.

    Product
    Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to stabilize and secure a variety of catheters, surgical drains, and tubes from sizes 5-40 French.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0367-2021·2021-04-07

    J & J Distributing Recalls Tastebuds Layered Fiesta Taco Dip for Listeria Risk

    J & J Distributing Company is recalling Tastebuds Layered Fiesta Taco Dip due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in eight states.

    Product
    tastebuds Layered Fiesta Taco Dip, Net Wt. 9 oz. (255g), UPC 0 38232 31611 8, Distributed By H. Brooks & Co Mpls MN 55112
    Category
    Food
    Distribution
    8 states