Medtronic Forced to Recall Pump Over Battery Flaw
A Medtronic recall of the SynchroMed II Implantable Infusion Pump has been issued due to a battery flaw.
A Medtronic recall of the SynchroMed II Implantable Infusion Pump has been issued due to a battery flaw.
Due to side effects with long term use, such as femur fractures, the FDA will update the labels on Fosamax and other bisphosphonate drugs.
Due to the high number of reported vaginal mesh complications, the FDA is considered stricter regulations for those POP vaginal meshes.
Forced Placed Insurance Complaints: Some mortgage companies are allegedly forcing homeowners to purchase a costly, second flood insurance policy.
James Hardie siding issues, which include flaking and moisture problems, have led to failed expectations among consumers, according to a lawsuit against the manufacturer.
The FDA has released a safety alert warning consumers not to use the ShoulderFlex Massager, citing the risk of strangulation.
The FDA has released a warning that high doses of Celexa have been linked to an increased risk of abnormal changes in the activity of the heart.
Reportedly, a lawsuit was filed against American Medical Systems (AMS) and Boston Scientific for vaginal mesh complications.
Trimboard problems can reportedly include swelling, decay and rotting due to a manufacturing defect.
An Actos bladder cancer FDA warning has been released announcing that use of Actos longer than a year may be linked to bladder cancer.