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 ...

SHANGHAI/CHICAGO (Reuters) - Health agencies are investigating an outbreak of bloodstream infections in children from four U.S. states that may be linked to heparin and saline syringes made by Becton ...

The CDC confirmed 14 cases of bloodstream infections in children across four U.S. states that may be connected to heparin and saline syringes distributed by medical technology company Becton Dickinson ...

SHANGHAI/CHICAGO: Health agencies are investigating an outbreak of bloodstream infections in children from four U.S. states that may be linked to heparin and saline syringes made by Becton Dickinson ...

The U.S. Food and Drug Administration announced a nationwide recall of all lots of heparin and saline pre-filled flush syringes manufactured by AM2 PAT Inc., of Angier, N.C. Two lots have been found ...

The US Food and Drug Administration (FDA) recently announced recall of all lots of heparin and saline pre-filled flush syringes manufactured by AM2 PAT Inc., of Angier, N.C., after two lots were found ...

ANGIER, N.C., Dec. 21 (UPI) -- The U.S. Food and Drug Administration said a group of pre-filled heparin syringes produced by AM2 Pat Inc. has been recalled due to contamination. The recall of ...

The FDA on March 21 shared recommendations for healthcare organizations to conserve prefilled 0.9 percent sodium chloride intravenous lock/flush syringes amid a national shortage. 1. Use ...

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 ...

(Reuters) - Medical device maker Covidien Plc said it was recalling 14 lots of its Monoject prefill flush syringes sold in the United States and Bermuda as they contained non-sterilized water which ...