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Class Action Investigations

Class Action Investigations

Consumer complaints under attorney investigation; no lawsuits filed yet. When certain consumer complaints affect a larger number of individuals, an attorney may begin a class action investigation. The number of people affected in order to begin an investigation can and will vary depending on the nature of the product in question and the complaint involved. For example, a serious auto defect can lead to a loss of many lives and prompt a class action investigation based on a small number of complaints; a mislabeled food product might be recalled but not result in actual injury to anyone and, therefore, not prompt a class action investigation. If an attorney determines there is cause for legal action, a class action investigation can lead to a class action lawsuit being filed.

  • Nissan Recalls 468,815 Nissan Rogues
    Nissan Recalls 468,815 Nissan Rogues
    January 29 2015

    Los Angeles, CA: Nissan North America, Inc. (Nissan) is recalling 468,815 model year 2008-2013 Nissan Rogue vehicles manufactured March 7, 2007, to November 26, 2013, and 2014 Nissan Rogue Select vehicles manufactured September 23, 2013, to July 2...

  • Nissan Recalls 170,665 Pathfinder and Infinti Vehicles
    Nissan Recalls 170,665 Pathfinder and Infinti Vehicles
    January 29 2015

    Los Angeles, CA: Nissan North America, Inc. (Nissan) is recalling 170,665 model year 2013-2014 Nissan Pathfinder vehicles manufactured June 20, 2012, to November 18, 2013, 2014 Nissan Pathfinder Hybrid vehicles manufactured July 18, 2013, to...

  • Volkswagen Group of America Recalls 26,008 Vehicles
    Volkswagen Group of America Recalls 26,008 Vehicles
    January 27 2015

    Los Angeles, CA: Volkswagen Group of America, Inc. (Volkswagen) has issued a recall for certain model year 2011-2012 Audi S4, S5, Q7, 2012 Audi A6, Volkswagen Touareg Hybrid, and 2012-2013 Audi A7 vehicles. In the affected vehicles the fuel...

  • Dementia Drug Aricept Labeling to Include New Side Effect Warnings
    Dementia Drug Aricept Labeling to Include New Side Effect Warnings
    January 21 2015

    Los Angeles, CA: Health Canada has added new warnings to the prescribing information for the Alzheimer' drug Aricept (donepezil) advising of the risk of two rare but potentially serious conditions: muscle breakdown (rhabdomyolysis) and a...

  • Reports of Injury Prompt Recall of SKLZ Recoil 360 Resistance Trainers
    Reports of Injury Prompt Recall of SKLZ Recoil 360 Resistance Trainers
    January 12 2015

    Los Angeles, CA: About 52,000 units of the SKLZ Recoil 360™ All-Position Resistance Trainers are being recalled following reports of serious injuries. A weld on a ring on the resistance trainer' belt can break during use and cause the resistance...

  • Keurig Recalls MINI Plus Brewing Systems Due to Burn Hazard
    Keurig Recalls MINI Plus Brewing Systems Due to Burn Hazard
    December 24 2014

    Los Angeles, CA: A Keurig has issued a recall of its MINI Plus Brewing Systems because the water can overheat during brewing, spray out and burn consumers. So far, the Keurig has received about 200 reports of hot liquid escaping from the brewer...

  • Woman Dies After Taking Forza Raspberry Keytones
    Woman Dies After Taking Forza Raspberry Keytones
    December 11 2014

    Los Angeles, CA: A 24-year old woman has died from a heart attack after taking a large amount of a herbal dietary supplement called Forza raspberry ketones. The young woman was a health worker in the UK, and after taking her first dose of the...

  • Ziprasidone Linked to Rare But Potentially Fatal Skin Reactions
    Ziprasidone Linked to Rare But Potentially Fatal Skin Reactions
    December 11 2014

    Los Angeles, CA: The Food and Drug Association (FDA) is warning that the antipsychotic drug ziprasidone (marketed under the brand name, Geodon, and its generics) is associated with a rare but serious skin reaction that can progress to affect...

  • FDA Issues Class I Recall of CONMED Defibrillation Electrodes due to Risk of Death or Injury
    FDA Issues Class I Recall of CONMED Defibrillation Electrodes due to Risk of Death or Injury
    December 4 2014

    Los Angeles, CA: The Food and Drug Administration has classified this as a Class 1 Recall, the most serious recall where there is a reasonable risk of serious adverse health consequences or death, for certain PadPro and R2 Multi-function...

  • Nissan Infiniti Q70 Hybrid Vehicles Recalled
    Nissan Infiniti Q70 Hybrid Vehicles Recalled
    November 12 2014

    Los Angeles, CA: Nissan North America, Inc. (Nissan) is recalling certain model year 2014 Infiniti Q50 hybrid vehicles manufactured December 10, 2012, to June 25, 2014, and Infiniti Q70 hybrid vehicles manufactured November 7, 2013, to May 7, 2014...

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