Bayer and FDA informed healthcare professionals of the market withdrawal of the current liquid formulation of Leukine, a growth factor that helps fight infection and disease in appropriate patients by enhancing immune cell function.
The product was withdrawn because of an upward trend in spontaneous reports of adverse reactions, including syncope (fainting), which are temporally correlated [...]

MOM Enterprises Inc., and FDA informed consumers and healthcare providers that Baby’s Bliss Gripe Water, apple flavor, with a code of 26952V and expiration date of October 2008 (10/08) is being recalled due to the presence of Cryptosporidium infection.
The product is labeled Baby’s Bliss. Pediatrician Recommended Gripe Water. Apple Flavor. An herbal supplement used [...]

Bodee LLC, the maker of Zencore announced today that it is conducting a voluntary nationwide recall of all the company’s supplement product sold under the name Zencore Tabs.
Customers who have this product in their possession should stop using it immediately and contact their physician if they have experienced any problems that may be related [...]

Defibtech and FDA notified healthcare professionals of a worldwide recall of 42,000 Lifeline and ReviveR AEDs with software versions 2.002 and earlier.
The self-test software may allow a self-test to clear a detected low battery condition. The operator may be unaware of the low battery and the device may not deliver a defibrillation shock, resulting in [...]

Davol/Bard and FDA notified healthcare professionals of an expanded
recall and withdrawal of Large Oval and Large Circle patches. There is a
risk that the ring welds could break under stress placed on these
products during placement, which could potentially lead to patient
complications such as abdominal pain, bowel perforation or chronic
enteric fistulas.
Davol is expanding the voluntary recall of [...]