Tylenol Recall on 8 Hour Caplets – 50 Count

McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling one product lot of Tylenol 8 Hour caplets 50 count bottles as of October 18, 2010. The product, sold in the United States and Puerto Rico, is being recalled due to a small number of complaints of a musty or moldy odor. The odor is thought… Continue reading Tylenol Recall on 8 Hour Caplets – 50 Count

Recall of Select Heartstart Fr2+ AEDs

Official Press Release September 28, 2009 – Seattle – Philips announced today that it is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs). This recall is being conducted due to the possibility of a memory chip failure that may render the device inoperable. Only certain HeartStart FR2+ AEDs (models M3860A and M3861A, distributed… Continue reading Recall of Select Heartstart Fr2+ AEDs

LifePak CR Plus recall – Fire Service Alerts and Advisories from the U.S. Fire Administration

Medical Device Recall: LifePak CR Plus Automated External Defibrillators Audience: Emergency medical personnel, other healthcare professionals Physio Control, Inc., issued a recall of LifePak CR Plus Automated External Defibrillators (AED), used by emergency or medical personnel to treat adults in cardiopulmonary arrest. The product was recalled because the AED instructs the responder by voice prompts… Continue reading LifePak CR Plus recall – Fire Service Alerts and Advisories from the U.S. Fire Administration