SCHAUMBURG, Ill.--(BUSINESS WIRE)--APP Pharmaceuticals, Inc., a wholly owned subsidiary of Fresenius Kabi Pharmaceuticals Holding, Inc. (NASDAQ:APCVZ), announced today that it has received clearance ...

WASHINGTON, Aug. 20 (UPI) -- Covidien, a healthcare products producer, initiated a voluntary recall of certain lots of Monoject prefill flush syringes, U.S. government officials say. The U.S. Food and ...

The FDA has now concluded that there is sufficient capacity on the part of other suppliers that Baxter's recall will not jeopardize access to this drug, and has told Baxter that the company can now ...

January 22, 2008 — A nationwide recall has been expanded to include all lots of heparin and saline prefilled flushes made by AM2 PAT Inc, the US Food and Drug Administration (FDA) warned healthcare ...

Deerfield, IL - Baxter International is now recalling from the market all remaining lots and doses of its heparin sodium multidose and single-dose vials for injection and its heparin lock flush ...

APP also did not show that it investigated whether other batches may have been out of spec. "We are also concerned about a potentially related trend of OOS assay results for other batches of heparin ...

A mass recall of heparin has health-care providers concerned about supplies of the blood thinner that is used to clear intravenous lines and prevent clots in surgical and dialysis patients. Baxter ...

The US Food and Drug Administration’s (FDA) Center for Devices and Radiological Health (CDRH) issued final guidance Wednesday to aid manufacturers in reducing the risk of patient injury associated ...

The US Food and Drug Administration (FDA) has warned medical device maker Becton Dickinson (BD) for good manufacturing practice (GMP) violations at the company’s Franklin, Wisconsin facility. The ...

The U.S. Pharmacopeial Convention (USP) has revised its current standards on heparin labeling requirements to address safety concerns about the expression of drug strength. The labeling sections for ...