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.

54701–54725 of 81678

  • ModerateFDA (Devices)·Z-1575-2016·2016-05-04

    Mindray Panorama Patient Monitoring Network Recalled for Date Reversion

    Mindray DS USA is recalling Panorama Patient Monitoring Network units that may revert to the year 2000 during Daylight Savings Time.

    Product
    Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient Monitoring can view recal time, store, print, graph and trend patient clinical and demographic data. The Panoram Patient Monitoring Network can sent independent alarm limits for data send by the bedside…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1570-2016·2016-05-04

    BD Trucount Absolute Counting Tubes Recalled for Lot Mixing

    Becton, Dickinson and Company is recalling one lot of BD Trucount tubes because some pouches may contain tubes from a different lot, presenting a low risk to patient safety.

    Product
    BD Trucount Absolute Counting Tubes: Model number: 340334 IVD; BD Trucount tubes are used for determining absolute counts of leucocytes in blood. BD Trucount tubes are designed for use with in vitro diagnostic products such as BD Tritest reagents, and a suitably equipped…
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-1564-2016·2016-05-04

    Hansen Medical Recalls Magellan Robotic Catheter Accessory Kits

    Hansen Medical is recalling eight Magellan Robotic Catheter Accessory Kits because one batch was radiated below the required dose.

    Product
    Magellan Robotic Catheter Accessory Kits, Model number MACC 50 and MACC80. Cardiology: The Hansen Medical Magellan System is a robotic control system that enables positioning and visualization of a Magellan Catheter and an off-the-shelf guide wire while allowing a physician…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1261-2016·2016-05-04

    Family Gourmet Brown Rice Recalled Due to Live Insects

    Family Dollar is recalling Family Gourmet Natural Whole Grain Brown Rice because live insects were found in unopened bags.

    Product
    Family Gourmet Natural Whole Grain Brown Rice, 32 oz. (2 lb.) plastic bag (SKU: 1230394)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1527-2016·2016-05-04

    Corin Trinity Acetabular Shell Recalled for Packaging Abrasion Risk

    Corin USA Limited is recalling 629 Trinity Acetabular Shell devices used in total hip replacements due to a potential for abrasion of the sterile barrier pouches in the new packaging system.

    Product
    Trinity Acetabular Shell Product Usage: Total Hip Replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1246-2016·2016-05-04

    Bissinger's Milk Chocolate Eggs Recalled for Mislabeling Artificial Vanillin as Vanilla

    Karl Bissinger, LLC is recalling Bissinger's Milk Chocolate Eggs because the product contains artificial vanillin but is labeled as containing vanilla.

    Product
    Bissinger's Milk Chocolate Eggs packaged in 6.5 oz (UPC 846107009382) Item: #11108 or 1 lb. (UPC 846107003458) Item: # 111049 plastic bags. Bissinger's Handcrafted Chocolatier, St. Louis, MO.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1526-2016·2016-05-04

    Corin Trinity Acetabular System Recalled for Packaging Abrasion Risk

    Corin USA Limited is recalling 629 Trinity Acetabular System devices due to potential abrasion of sterile barrier pouches in the new packaging system.

    Product
    Trinity Acetabular System Product Usage - Total Hip Replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1576-2016·2016-05-04

    Drew Scientific Recalls Drew3-PAC Reagent Packs Due to Platelet Background Issues

    Jas Diagnostics/Drew Scientific is recalling Drew3-PAC reagent packs because they may cause elevated platelet background during routine analyzer checks.

    Product
    Drew Scientific Inc. Drew3-PAC. This D3 Reagent Pack includes: diluent reagent 5L, enzymatic cleaner 750 mL, and a lysing reagent 125 mL.
    Category
    Medical Device
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-1566-2016·2016-05-04

    Stryker PneumoSure Insufflators Recalled for Flow Rate Drop

    Stryker Endoscopy is recalling PneumoSure insufflators because the flow rate drops to zero when connected to a house gas source, suspending insufflation.

    Product
    PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator; High pressure units (HPU) (40L and 45L). Model Numbers: 620-040-610, 620-040-611, 620-040-613, 620-040-614, 620-040-600, 620-040-601, 620-040-602, 620-040-604, 105-210-684 The Pneumo Sure XL High…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1582-2016·2016-05-04

    Teleflex Pleur-evac Chest Drainage System Recalled for Missing Tyvek Bag Label

    Teleflex Medical is recalling Pleur-evac Chest Drainage Systems because the Tyvek bag label is missing, preventing identification of material code, lot number, and expiration date.

    Product
    Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product Usage: Pleur-Evacs are sterile, single-use, chest drainage systems intended for post-operative use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0834-2016·2016-05-04

    SKY Aspirin Chewable Tablets Recalled for Incorrect Outer Carton Labeling

    McKesson Packaging Services is recalling SKY Aspirin Chewable Tablets because the outer cartons were incorrectly labeled. The recall addresses a labeling mix-up.

    Product
    SKY Aspirin Chewable Tablets, 81 mg, Unit Dose 750 tablets (25 x 30) box, OTC, Distributed by: McKesson Packaging Service, Concord, NC 28027, NDC 63739-434-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V265000·2016-05-03

    Blue Bird Recalls 2017 Transit Buses Due to Seat Separation Risk

    Blue Bird is recalling specific 2017 Vision and All American transit buses because child seats may separate from the base frame due to bolt failure.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V267000·2016-05-03

    Forest River Recalls 2007-2014 Solera and Coachmen Prism RVs

    Forest River is recalling 2007-2014 Solera and Coachmen Prism vehicles because the driver's air bag inflator may rupture during deployment, potentially causing serious injury.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN SOLERA, PRISM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16155·2016-05-03

    Cascade Designs Recalls Avalanche Rescue Probes Due to Suffocation Risk

    Cascade Designs is recalling Striker 320 and 240 avalanche rescue probes because a lock button failure may prevent the probe from extending, posing a suffocation hazard.

    Product
    Avalanche rescue probes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V266000·2016-05-03

    Adkins Recalls 2013-2016 Dominator Trucks Due to Crane Cover Defect

    Adkins is recalling 2013-2016 Dominator trucks equipped with specific IMT cranes because the valve bank cover may crack and fall off, creating a road hazard.

    Product
    ADKINS — ADKINS DOMINATOR II, DOMINATOR I, DOMINATOR III, DOMINATOR-PROPANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V262000·2016-05-02

    QT Equipment Recalls 2013-2016 Dominator Trucks Due to Crane Cover Defect

    QT Equipment is recalling 2013-2016 Dominator trucks because a crane valve bank cover may crack and fall off, creating a road hazard.

    Product
    QT EQUIPMENT — QT EQUIPMENT DOMINATOR III, DOMINATOR-PROPANE, DOMINATOR II, DOMINATOR I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V260000·2016-04-29

    Thor Motor Coach Recalls 2017 ACE and Road Bear Rental Motorhomes

    Thor Motor Coach is recalling 2017 ACE and Road Bear Rental motorhomes because seat belt anchorages in the slide-out section may pull loose during a crash.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ROAD BEAR RENTAL, ACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V261000·2016-04-29

    Mercedes-Benz and Freightliner Sprinter Vans Recalled for Window Separation Risk

    Daimler Vans USA is recalling 2015-2016 Mercedes-Benz and Freightliner Sprinter vans because multiple paint layers may cause windows to separate in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V259000·2016-04-29

    Monroe Truck Equipment Recalls 2013 Ford F-550 Trucks with IMT Cranes

    Monroe Truck Equipment is recalling one 2013 Ford F-550 truck equipped with an IMT crane because the valve bank cover may crack and fall off, creating a road hazard.

    Product
    MONROE — MONROE FORD F-550 W/IMT CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V258000·2016-04-29

    Forest River Cardinal RVs Recalled for Incorrect Tire Placard Information

    Forest River is recalling 2016-2017 Cardinal RVs because the tire placard lists incorrect tire and rim specifications, which could lead to under-inflation and tire blowouts.

    Product
    FOREST RIVER — FOREST RIVER CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16C005000·2016-04-29

    Kiddy USA Recalls World Plus Child Seats Due to Buckle Defect

    Kiddy USA is recalling World Plus child seats because the harness buckle may not fully latch, increasing injury risk in a crash.

    Product
    CHILD SEAT:HARNESS/CROTCH BUCKLE recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide