The personal injury attorneys at Ligori & Sanders, Attorneys at Law are dedicated to keeping consumers safe. Below is a list of the most recent FDA recalls that may affect our clients and community.

Baxter Initiates Voluntary Recall of Two Lots of Dual Luer Lock Caps (September 19, 2013)

Baxter International Inc. announced today it has initiated a voluntary recall of two lots of its Dual Luer Lock Caps (Product Code 2C6250, Lots 10043 and 10044) because of the presence of loose particulate matter found in the packaging. The U.S. Food and Drug Administration (FDA) has designated this as a Class I recall.

Read more about the Baxter Dual Lucer Lock Caps Recall

FDA limits acetaminophen in prescription combination products; requires liver toxicity warnings (January 13, 2011)

The U.S. Food and Drug Administration is asking manufacturers of prescription combination products that contain acetaminophen to limit the amount of acetaminophen to no more than 325 milligrams (mg) in each tablet or capsule.

Read more about the dangers of acetaminophen and liver damage