The Recall Desk

State

Minnesota product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42676–42700 of 81660

  • ModerateFDA (Devices)·Z-1804-2018·2018-05-23

    Beckman Coulter Recalls MicroScan MICroSTREP Plus Panel Due to QC Failures

    Beckman Coulter is recalling 523 boxes of MicroScan MICroSTREP Plus Panel and associated broth due to quality control testing failures.

    Product
    BECKMAN COULTER MicroScan MICroSTREP Plus Panel, MicroScan Mueller-Hinton Broth with 3% lysed horse blood, Catalog Number 81015 MicroScan Mueller Hinton Broth with 3% Lysed Horse Blood is used for inoculation of MicroScan MICroSTREP plus and MicroFAST panels. MICroSTREP plus…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1888-2018·2018-05-23

    Ethicon 5mm Endopath Xcel Trocar Recalled for Lubrication Defect

    Ethicon Endo-Surgery Inc is recalling 5mm Endopath Xcel trocars due to insufficient lubrication, which may prolong surgery or introduce minute particles.

    Product
    5mm Endopath Xcel with Optiview Technology, Universal Trocar with Stability Sleeve, 5mm, 100mm shaft length, 2CB5LT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1885-2018·2018-05-23

    Ethicon Endo-Surgery Recalls 5mm Endopath Xcel Trocars Due to Lubrication Issues

    Ethicon Endo-Surgery is recalling 5mm Endopath Xcel trocars because insufficient lubrication may prolong surgery or risk introducing minute particles.

    Product
    5mm Endopath Xcel with Optiview Technology, Bladeless Trocar with Stability Sleeve, 5mm, 100mm shaft length, 2B5LT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1886-2018·2018-05-23

    Ethicon 5mm Endopath Xcel Trocar Recalled for Insufficient Lubrication

    Ethicon Endo-Surgery is recalling 5mm Endopath Xcel trocars because insufficient lubrication may prolong surgery or introduce minute particles.

    Product
    5mm Endopath Xcel with Optiview Technology, Bladeless Trocar with Stability Sleeve, 5mm, 75mm shaft length, 2B5ST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1802-2018·2018-05-23

    Bard Peripheral Vascular Seeker Crossing Support Catheter Recalled for Endotoxin Risk

    Bard Peripheral Vascular Inc is recalling 140 units of the Seeker Crossing Support Catheter due to potential bacterial endotoxin on packaging hoops.

    Product
    BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter, 0.035", 150 cm, REF SK15035M. Intended to support a guidewire during access into the vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0802-2018·2018-05-23

    Sun Pharma Recalls Sulfamethoxazole and Trimethoprim Tablets Due to Foreign Matter

    Sun Pharmaceutical Industries is recalling one lot of Sulfamethoxazole and Trimethoprim tablets because polyethylene was detected in two tablets.

    Product
    SULFAMETHOXAZOLE AND TRIMETHOPRIM — SULFAMETHOXAZOLE AND TRIMETHOPRIM (SULFAMETHOXAZOLE AND TRIMETHOPRIM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0815-2018·2018-05-23

    Pharmalucence Recalls Technetium TC 99M Mebrofenin Kits for Stability Failures

    Pharmalucence, Inc. is recalling Technetium TC 99M Mebrofenin kits nationwide because they failed stability specifications.

    Product
    KIT FOR THE PREPARATION OF TECHNETIUM TC 99M MEBROFENIN — KIT FOR THE PREPARATION OF TECHNETIUM TC 99M MEBROFENIN (KIT FOR THE PREPARATION OF TECHNETIUM TC 99M MEBROFENIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1893-2018·2018-05-23

    Beckman Coulter Recalls iChem VELOCITY Urine Chemistry Strips Due to Defect

    Beckman Coulter is recalling a subset of iChem VELOCITY Urine Chemistry Strips because an incorrect pad may cause false negative results for leukocytes.

    Product
    iChem VELOCITY Urine Chemistry Strips, REF 800-7212 Product Usage: The iChem VELOCITY automated urine chemistry system is an in vitro diagnostic deice used to automate the urine chemistry analysis profile using iChem VELOCITY Urine Chemistry Strips. The iChem VELOCITY can be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·040-2018·2018-05-23

    Uno Foods Recalls Ham and Cheese Calzones Due to Misbranding

    Uno Foods Inc. is recalling 1,881 pounds of ham and cheese calzones because the packages contain buffalo chicken calzones instead.

    Product
    Great Kitchens Food Company — Uno Foods Inc. Recalls Ham and Cheese Calzones Due to Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0803-2018·2018-05-23

    Boiron Recalls Calendula Cream Due to Outer Carton Labeling Error

    Boiron Inc. is recalling 52,810 tubes of Calendula Cream because the outer carton incorrectly lists the active ingredient concentration as 7% instead of 10%.

    Product
    Calendula Cream, calendula officinalis 1X HUS-10%, 2.5 oz. tubes, Distributed by Boiron Inc., Newtown Square, PA
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0818-2018·2018-05-23

    Sun Pharma Recalls Riomet Metformin Solution Due to Labeling Errors

    Sun Pharmaceutical Industries is recalling Riomet (metformin hydrochloride) oral solution due to identified labeling discrepancies in the patient literature.

    Product
    RIOMET — RIOMET (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·18E036000·2018-05-22

    Fuel Helmets Recalls Open Face Helmets for Impact Protection Failure

    Fuel Helmets is recalling specific Open Face helmets that may not adequately protect the wearer's head in an impact, increasing the risk of injury.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18162·2018-05-22

    Porsche Recalls Wooden Toy Cars Due to Choking Hazard

    Porsche is recalling My First Porsche wooden toy cars because wheels and axles can detach, posing a choking hazard to young children.

    Product
    My First Porsche - Wooden Cars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V334000·2018-05-21

    2019 Coachmen Recreational Trailers Recalled for Incorrect Tire Placard

    Forest River is recalling 2019 Coachmen Clipper and Viking trailers because the Federal Placard lists incorrect tire pressure, which could lead to underinflation and tire failure.

    Product
    COACHMEN — COACHMEN CLIPPER, VIKING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V365000·2018-05-18

    Van-Con Recalls One 2016 School Bus Due to Roof Panel Bonding Defect

    Van-Con is recalling one 2016 33803 Dual Rear Wheel school bus because roof panel seams were not correctly bonded, posing an increased injury risk in a crash.

    Product
    VAN-CON — VAN-CON 33803 DUAL REAR-WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V332000·2018-05-17

    Chrysler Recalls Vehicles for Cruise Control Disengagement Defect

    Chrysler is recalling over 4.8 million vehicles because a wiring short may prevent the cruise control system from disengaging, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER, DODGE, JEEP 300, JOURNEY, CHARGER, 200
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E033000·2018-05-17

    LuK Hybrid Propulsion System Recall for Fire Risk

    LuK is recalling hybrid propulsion systems where oil accumulation may cause an electrical short and increase fire risk. Dealers will inspect and replace components free of charge.

    Product
    HYBRID PROPULSION SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V330000·2018-05-17

    Thomas Built Buses Recalls Minotour Transit Buses for Wheelchair Lift Defect

    Daimler Trucks North America is recalling 2003-2006 Thomas Built Buses Minotour transit buses because a missing relay may allow the wheelchair lift to operate while the vehicle is moving, increasing injury risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide