Adverse Event Reporting Program News Today

The Arrow FiberOptix and UltraFlex Intra-Aortic Balloon (IAB) Catheter Kits are being recalled for manufacturing issues that may prevent full balloon inflation and cause patient harm

Elekta Instrument AB recalls disposable biopsy needle kit for Leksell Stereotactic System for possibly containing microscopic stainless steel debris on the inside of the biopsy needle

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death

Important Recall Notice: AvKARE recalls Atovaquone Oral Suspension due to potential Bacillus cereus contamination. Learn about risks, recommendations, and how to proceed if you have this product.

Food and water safety information for consumers during hurricanes, power outages, and flooding.

/PRNewswire/ -- It is important to keep food safety in mind when handling eggs. Eggs are a popular food all year long, and especially popular during this time...

The U.S. Food and Drug Administration (FDA) announced that Abbott is recalling its HeartMate Touch System (version 1.0.32) for risk of unexpected pump stop or start. Issues may occur if the HeartMate Touch System is disconnected from a patient’s HeartMate Controller while a “pump stop” command is running. People who have the implantable HeartMate 3 Left Ventricular Assist Device may be affected.

Please be aware, this recall is a correction, not a product removal.

The FDA has issued a warning urging consumers not to purchase or use tianeptine products due to serious risks

This new warning for consumers cautions against use of Rebright, South Moon, or FivFivGo eye drops as a result of potential eye infection risks.