A software defect in Baxter’s Dose IQ Software version 9.0.x may impact how fluid is delivered to a patient with the Spectrum IQ Infusion Pump

Increased risk of neurological adverse events, mortality and possible failure of the pump to restart led to stop sale and distribution of HeartWare HVAD System

[eBay Seller ID: jongu 4308] is voluntarily recalling all lots of Hydro Pineapple Burn to consumer level. FDA analysis has found the product to contain undeclared sibutramine. Sibutramine was an FDA approved drug used as an appetite suppressant for weight loss but was withdrawn from the market beca

There is likely a high risk of false results using these tests. The tests are not FDA authorized, cleared, or approved.

Boston Scientific recalls INGENIO Family of Pacemakers and CRT-Ps, used to treat slower than normal heartbeats and heart failure, due to the risk of transitioning to safety mode.

SterRx, LLC today announced the voluntary nationwide recall of three lots of Sodium Bicarbonate in 5% Dextrose Injection 150mEq per 1,000 mL due to waterborne microbial contamination. SterRx, LLC has initiated this voluntary recall of Sodium Bicarbonate injection, to the Hospital Pharmacy level.