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.

Which agencies issued them

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.

48926–48950 of 81668

  • SevereFDA (Devices)·Z-1503-2017·2017-03-29

    Ohmeda Medical Spot PT Lite Phototherapy System Recalled for Power Cord Fire Risk

    Ohmeda Medical is recalling Spot PT Lite Phototherapy Systems because certain power cords could overheat, posing a risk of fire or thermal injury.

    Product
    Giraffe Spot PT Ohmeda Medical Spot PT Lite Phototherapy System- The Spot PT Lite Phototherapy System provides light therapy for the treatment of hyperbilirubinemia, commonly known as neonatal jaundice, during the newborn period in the hospital
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1504-2017·2017-03-29

    Ohmeda Medical Recalls Giraffe OmniBed Infant Incubators Due to Fire Risk

    Ohmeda Medical is recalling Giraffe OmniBed infant incubators and warmers because certain power cords may overheat, posing a risk of fire or thermal injury.

    Product
    Giraffe OmniBed Ohmeda Medical Giraffe OmniBed- The OmniBed is a combination of an infant incubator and an infant warmer. The device can be operated as an incubator or as a warmer and can transition from one mode to the other on user s demand. It cannot be operated in both…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1654-2017·2017-03-29

    Sargento Artisan Blends Double Cheddar Shredded Cheese Recalled for Listeria Risk

    Sargento Foods is recalling specific lots of Artisan Blends Double Cheddar Shredded Cheese due to potential Listeria monocytogenes contamination.

    Product
    Sargento Artisan Blends Double Cheddar Shredded Cheese, 8oz., UPC 4610040094, Sell By date: H09JUN17 and H08JUN17
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1510-2017·2017-03-29

    Ohmeda-Ohio CarePlus Incubator Recall Due to Power Cord Overheating Risk

    Ohmeda Medical is recalling CarePlus Incubators because certain power cords may overheat, posing a risk of fire or thermal injury.

    Product
    CarePlus Incubator Ohmeda-Ohio CarePlus Incubator- Incubators provide a controlled thermal environment for neonates who are unable to provide their own thermoregulation. They may also be used for short periods of time to facilitate the neonate s transition from the uterus to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1643-2017·2017-03-29

    Manzana Recalls Trader Joe's Apple Sauce Due to Glass Fragments

    Manzana Products Co. is recalling Trader Joe's First Crush Unsweetened Gravenstein Apple Sauce because small pieces of glass were found in the product.

    Product
    Trader Joe's First Crush Unsweetened Gravenstein Apple Sauce; 24 oz. glass jar. Best Before date stamped on top of lid. UPC:00015905 Distributed by Trader Joe's, Monrovia, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1502-2017·2017-03-29

    Ohmeda Giraffe Incubator Recall Due to Power Cord Overheating Risk

    Ohmeda Medical is recalling Giraffe Incubators because certain power cords may overheat, posing a fire or thermal injury risk.

    Product
    Giraffe Incubator The Giraffe Incubator is an infant incubator. Incubators provide heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Incubators provide an enclosed temperature controlled environment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1645-2017·2017-03-29

    Sargento Shredded Cheese Recalled for Listeria Contamination Risk

    Sargento Foods is recalling specific lots of Shredded Nacho & Taco Cheese due to potential Listeria monocytogenes contamination.

    Product
    Sargento Chef Blends Shredded Nacho & Taco Cheese, 8 oz., UPC 4610040041.,Sell By dates of H14JUN17, H12JUL17, H04MAY17, S15MAY17, H01JUN17.
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1511-2017·2017-03-29

    Ohmeda Infant Warmer System Recalled Due to Overheating Power Cords

    Ohmeda Medical is recalling IWS Infant Warmer Systems because certain power cords may overheat, posing a fire and thermal injury risk.

    Product
    IWS Infant Warmer System-Infant radiant warmers provide infrared heat, in a controlled manner, to neonates who are unable to thermoregulate based on their own physiology or necessitate external heat to smoothen the transition from the uterus to the external environment. They…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1507-2017·2017-03-29

    Ohmeda Infant Warmers Recalled Due to Power Cord Overheating Risk

    Ohmeda Medical is recalling Giraffe and Panda infant radiant warmers because certain power cords may overheat, posing a fire or thermal injury risk.

    Product
    Giraffe Bedded Warmer, Panda Warmer Modification to Giraffe and Panda Warmers (Giraffe and Panda Uninterruptible Power Supply) - Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1508-2017·2017-03-29

    Ohmeda Infant Radiant Warmers Recalled for Power Cord Overheating Risk

    Ohmeda Medical is recalling Giraffe and Panda infant radiant warmers because certain power cords could overheat, posing a risk of fire or thermal injury.

    Product
    Giraffe Bedded Warmer, Panda Warmer Modifiction to Giraffe and Panda Warmer- Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Infant radiant warmers may be used to facilitate the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0606-2017·2017-03-29

    Legacy Pharmaceutical Recalls Atenolol Tablets Due to Foreign Tablet Presence

    Legacy Pharmaceutical Packaging LLC is recalling 48,012 bottles of atenolol 50 mg tablets because a customer reported finding a paroxetine 20 mg tablet inside a bottle.

    Product
    ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The Kroger Co., 1014 Vine Street, Cincinnati, OH 45202; Manufactured for: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1625-2017·2017-03-29

    Diamond Crystal Baking Powder Recalled for Potential Metal Contamination

    Diamond Crystal Brands is recalling 1,033 cases of 5 lb. baking powder because metal pieces were found missing from a sifter screen during sanitation.

    Product
    Baking Powder Net Wt. 5 lbs. (2.27 kg) packaged 6 bags per case, under the following brand names: Chef's Companion UPC 50719098580015, Diamond Crystal Brands, Inc. Savannah, GA 31405; and Sysco UPC 10074865238813, distributed by Sysco Corporation, Houston, TX 77077-2099.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1520-2017·2017-03-29

    CareFusion Alaris System PC Unit Recall for Battery Alarm Failure

    CareFusion is recalling Alaris System PC units because low battery alarms may fail to trigger before the battery discharges, stopping all infusion channels.

    Product
    Alaris System PC unit, model no. 8000 and 8015. The central programming, monitoring and power supply component for the Alaris infusion pump System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1498-2017·2017-03-29

    Merge Eye Station Import Utility Recalled for System Lockup Risk

    Merge Healthcare is recalling the Eye Station Import Utility software because system lockups may cause patient injury or delay diagnosis.

    Product
    Merge Eye Station Import Utility (ESIU). The firm name on the labeling is Merge Healthcare.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1517-2017·2017-03-29

    Merge Healthcare Recalls Merge Cardio Software Due to Data Integrity Issues

    Merge Healthcare is recalling Merge Cardio software versions 9.0 through 9.0.8 because users can merge device files with confirmed reports, potentially adding unverified information.

    Product
    Merge Cardio software. Product Usage: Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1627-2017·2017-03-29

    Diamond Crystal Cocoa Powder Recalled for Potential Metal Contamination

    Diamond Crystal Brands is recalling Chef's Companion Natural Cocoa Powder because metal pieces were found missing from a sifter screen during sanitation.

    Product
    Natural Cocoa Powder 22-24% cocoa butter, Net Wt. 5 lbs. (2.27 kg) packaged under the following brand name: Chef's Companion: 1 bag /case, UPC 10719098582240; Diamond Crystal Brands, Inc. Savannah, GA 31405
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1499-2017·2017-03-29

    Stanley Security Recalls 500 Arial Wireless Call Pendants

    Stanley Security Solutions is recalling 500 Arial Wireless Water-Resistant Call Pendants because they were incorrectly programmed, which may prevent alarms from sounding when the button is pressed.

    Product
    Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is part of the Arial wireless emergency call management system. It enables residents in assisted living, skilled nursing or independent living to call staff with the press of a button.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1494-2017·2017-03-29

    Nidek EC-5000 Excimer Laser Software Recall for Unintended Correction Programming

    Nidek Inc is recalling Final Fit Software versions 1.11 and 1.12 for the EC-5000 Excimer Laser System because treatment planning could be programmed with an unintended correction.

    Product
    Final Fit Software Version 1.11 and 1.12; PC Based software installed outside Nidek EC-5000 Excimer Laser System. Ophthalmic laser system use for correction of corneal refraction and ablation of the corneal surface. The system is composed of a laser generator which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1626-2017·2017-03-29

    Diamond Crystal Cocoa Powder Recalled for Potential Metal Contamination

    Diamond Crystal Brands is recalling specific lots of Natural Cocoa Powder because metal pieces were found missing from a sifter screen during sanitation.

    Product
    Natural Cocoa Powder 10-12% cocoa butter, Net Wt. 5 lbs. (2.27 kg) packaged under the following brand names: Monarch distributed by U.S. Foodservice UPC 50758108102533; Chef's Companion: 1 bag /case, UPC 10719098582233; and 6 bags/case, UPC 50719098582293 Diamond Crystal…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V217000·2017-03-29

    2016 Thomas Built Buses Saf-T-Liner C2 Recalled for Transmission Defect

    Daimler Trucks North America is recalling one 2016 Thomas Built Buses Saf-T-Liner C2 school bus because the transmission grade brake may fail to deactivate, increasing crash risk in slippery conditions.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17120·2017-03-29

    Juratoys Recalls Janod Push Toy Trolleys Due to Impact Injury Hazard

    Juratoys is recalling four models of Bricolo by Janod push toy trolleys because they can tip backwards, posing an impact injury hazard to children.

    Product
    Bricolo by Janod ® Push toy trolleys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1539-2017·2017-03-29

    Integra Recalls Panta Nails Due to Potential Sterility Seal Issues

    Integra LifeSciences is voluntarily recalling Panta and Panta XI Nails because package seals may not maintain intended sterility.

    Product
    Panta Nail, Rx only, Sterile,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1642-2017·2017-03-29

    Manzana Recalls Trader Joe's Apple Sauce Due to Glass Fragments

    Manzana Products Co. is recalling Trader Joe's Organic Unsweetened Apple Sauce after customer complaints and inspections revealed small pieces of glass in the product.

    Product
    Trader Joe's Organic Unsweetened Apple Sauce; 24 oz. glass jar. Best Before date stamped on top of lid. UPC: 00194877 Distributed by Trader Joe's, Monrovia, CA
    Category
    Food
    Distribution
    Distributed nationwide