Recalls for Myocardial Infarction

SLIM-K Capsules by Bethel Nutritional Consulting, Inc.: Recall - Undeclared Drug Ingredients
12/22/2014 Medical Recall

Can increase blood pressure and/or pulse rate, interact in life threatening ways with other medications, casue serious GI disturbances, irregular heartbeat, and cancer with long-term use.

  • Company:
    Bethel Nutritional Consulting, Inc.
Forever Beautiful Bee Pollen by REFA Enterprises: Recall - Undeclared Drug Ingredients
11/20/2014 Medical Recall

Risk for those with a history of coronary artery disease, congestive heart failure, arrhymias or stroke

  • Company:
    REFA Enterprises
Long-term Antiplatelet Therapy: Safety Announcement - Preliminary Trial Data Shows Benefits But a Higher Risk of Non-Cardiovascular Death
11/16/2014 Medical Recall

FDA believes the benefits of clopidogrel (Plavix) and prasugrel (Effient) therapy continue to outweigh their potential risks when used for approved uses.

  • Category
    Myocardial Infarction
Dream Body Slimming Capsule: Public Notification - Undeclared Drug Ingredient
01/22/2014 Medical Recall

Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke.

  • Category
    Myocardial Infarction
Nitroglycerin in 5% Dextrose Injection by Baxter: Recall - Particulate Matter
11/27/2013 Medical Recall

Voluntary recall of one lot due to particulate matter found in one vial. If infused, particulate matter could lead to potential venous and/or arterial thromboembolism.

  • Company:
    Baxter International Inc
Bard LifeStent Solo Vascular Stent: Class 1 Recall - Failure to Deploy
10/18/2013 Medical Recall

Serious adverse health consequences, including complications of bleeding, loss of limb, heart attack, or stroke.

  • Category
    Myocardial Infarction