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.

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.

55151–55175 of 81678

  • HighNHTSA·16E027000·2016-04-05

    Hale Recalls 6 Inch Suction Strainers Due to Soldering Defect

    Hale Products Inc. is recalling 6 Inch Suction Strainers manufactured between July 2015 and March 2016. Improper soldering may cause the strainer to break, potentially damaging fire pumps and increasing injury risk.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V191000·2016-04-05

    Nova Bus Recalls 2010-2015 LFS Transit Buses for Seat Belt Defect

    Nova Bus is recalling 2010-2015 LFS transit buses because missing welds on seat J-Brackets may allow seat belt anchorages to separate, increasing injury risk in a crash.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V189000·2016-04-04

    Kalmar Ottawa T2 Recalled for Inaccurate Brake Pressure Gauge

    Kalmar is recalling 2014-2016 Ottawa T2 vehicles because the brake system air pressure gauge may not display accurate levels, increasing crash risk.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E026000·2016-04-01

    Bosch Recalls Aftermarket Brake Pads for Ford, Lincoln, and Mercury Vehicles

    Bosch is recalling specific aftermarket front brake pads for 1993-2007 Ford, Lincoln, and Mercury vehicles because a shifting shim may damage the brake disc, potentially reducing braking power.

    Product
    FORD — FORD, LINCOLN, MERCURY TAURUS, TAURUS SHO, CONTINENTAL, SABLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V185000·2016-04-01

    Kompact Kamp Recalls Motorcycle Trailers Missing Side Marker Lights

    Kompact Kamp is recalling 1983-2016 Li'l Clipper motorcycle trailers manufactured without side marker lights, which may decrease visibility and increase crash risk.

    Product
    KOMPACT KAMP — KOMPACT KAMP LI'L CLIPPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V186000·2016-04-01

    Pierce Recalls 2010-2016 Vehicles Due to Flashlight Battery Fire Risk

    Pierce Manufacturing is recalling 2010-2016 Arrow-XT, Quantum, and Velocity vehicles because Pelican flashlights may overheat and cause a fire.

    Product
    PIERCE — PIERCE VELOCITY, QUANTUM, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V183000·2016-03-31

    Ford Recalls 2015-2016 Lincoln MKC and Explorer for Fire Risk

    Ford is recalling 2015-2016 Lincoln MKC and 2016 Ford Explorer vehicles because engine block heaters may overheat and cause a fire.

    Product
    LINCOLN — LINCOLN, FORD MKC, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E024000·2016-03-31

    Strategic Sports Recalls Leather Up XElement Motorcycle Helmets

    Strategic Sports is recalling specific Leather Up XElement motorcycle helmets that may not adequately protect users in a crash, failing federal safety standards.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16134·2016-03-31

    Gamewell-FCI Recalls Fire Alarm Panels Due to Failure to Alert

    Gamewell-FCI is recalling approximately 1,000 fire alarm panels because specific configurations may cause the system to fail to detect and respond to fire, smoke, or carbon monoxide alarms.

    Product
    Gamewell-FCI fire alarm panels (ILI-MB-E3 and ILI-S-E3)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16129·2016-03-31

    Manhattan Toy Recalls Busy Loops Table Top Toys Due to Choking Hazard

    The Manhattan Toy Company is recalling Busy Loops table top toys because plastic beads can break off, posing a choking hazard. No injuries have been reported.

    Product
    Busy Loops table top toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16735·2016-03-31

    Grosfillex Recalls Havana Commercial Side Chairs and Bar Stools

    Grosfillex is recalling Havana commercial side chairs and armless bar stools because the backrest can crack and detach, posing a fall hazard.

    Product
    Havana side chairs and armless bar stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16133·2016-03-31

    CE North America Recalls KUL Fan Heaters Due to Fire Hazard

    CE North America is expanding a recall of KUL fan heaters sold at H-E-B in Texas due to a fire hazard. One overheating incident was reported, with no injuries or property damage.

    Product
    KUL fan heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1242-2016·2016-03-30

    Siemens IMMULITE 1000 Estradiol Test Recalled for Faslodex Interference

    Siemens Healthcare Diagnostics is recalling IMMULITE 1000 Estradiol Test kits because the drug Faslodex may cause falsely elevated results.

    Product
    IMMULITE 1000 Estradiol Test Code E2 Catalog Number: LKE21, LKE21(D), LKE25 SMN: 10381132, 10702832, 10381142 Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers - for the quantitative measurement of estradiol in serum, as an aid in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0780-2016·2016-03-30

    Sagent Recalls Fluconazole Injection Due to Cross-Contamination with Metronidazole

    Sagent Pharmaceuticals is recalling specific lots of Fluconazole Injection due to cross-contamination with metronidazole. The affected product is distributed nationwide and in Puerto Rico.

    Product
    Fluconazole Injection, USP (in 0.9% Sodium Chloride), 200 mg per 100 ml, Single-Dose Container Bag, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195, NDC 25021-0113-82
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1220-2016·2016-03-30

    Recall of Bacteria-Contaminated Castile Soap Towelettes in Medical Kits

    The FDA is recalling specific lots of Aplicare Castile Soap towelettes found in medical kits due to bacterial contamination.

    Product
    Covidien Dover PRECSION PRM 14FR SIL FLY Item Code: ¿ PP14SD ¿¿ Castile soap towelettes are used to clean the genital area for male and female patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0790-2016·2016-03-30

    Nestle Recalls Lean Cuisine Spinach Artichoke Ravioli Due to Glass Contamination

    Nestle is recalling Lean Cuisine Spinach Artichoke Ravioli due to the potential presence of glass pieces. Consumers should stop eating the product and return it to the store.

    Product
    Lean Cuisine Marketplace Spinach Artichoke Ravioli, UPC 13800-55806, Keep Frozen. Net Wt. 9 oz (255g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1219-2016·2016-03-30

    Castile Soap Towelettes Recalled Due to Bacterial Contamination

    Covidien LLC is recalling Castile soap towelettes found in Foley trays and specimen kits because they are contaminated with bacteria.

    Product
    Covidien Dover 400 PREM U/M 18FR SLVR FLY Item Code: ¿¿¿ P4P18XSD Castile soap towelettes are used to clean the genital area for male and female patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V179000·2016-03-30

    Forest River Recalls Puma Trailers Due to Tire Clearance Defect

    Forest River is recalling 2008-2016 Puma recreational trailers and toy haulers because tires may contact the wheel well, risking deflation and loss of control.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide