Centurion Labs Ninjacof Liquid Recall [US]

US/Silver Spring: Centurion Labs recalls certain batch/lots of Ninjacof and Ninjacof A Liquids due to suspected Burkholderia Cepacia contamination and consequential risk of bacterial infection and illness, all serious health hazards. FDA: http://ht.ly/qCkV30eXS9R

Direct link: https://www.fda.gov/Safety/Recalls/ucm572873.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Drugs are subject to this recall:

Doctor Manzanilla Cough Syrup Recall [US]

US/Silver Spring: Mid Valley Pharmaceutical LLC recalls certain batch/lots of Doctor Manzanilla Cough & Cold and Doctor Manzanilla Allergy & Decongestant Relief Syrup due to suspected Burkholderia Cepacia contamination and consequential bacterial infection and illness, all serious health hazards. FDA: http://ht.ly/2HhS30eQFcs

Direct link: https://www.fda.gov/Safety/Recalls/ucm574250.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Drugs are subject to this recall:

Leader, Major Pharma & Rugby Labs Drug Recall [US]

US/Silver Spring: Leader Brand, Major Pharmaceuticals and Rugby Laboratories recalls all Liquid Drug products manufactured by PharmaTech LLC at its FDA-registered facility in Davie, Florida due to possible Burkholderia cepacia (“B. cepacia”) contamination, a serious health hazard. FDA: http://ht.ly/Shu430elrry

Direct link: https://www.fda.gov/Safety/Recalls/ucm571001.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Drugs are subject to this recall:

Rugby Labs Diocto Liquid & Syrup Recall [US]

US/Silver Spring: Rugby Laboratories recalls all current batch/lots of Diocto Liquid and Diocto Syrup manufactured by PharmaTech, LLC due to suspected Burkholderia cepacia contamination and consequential bacterial infection, a serious health hazard. FDA: http://ht.ly/732730ec2uq

Direct link: https://www.fda.gov/Safety/Recalls/ucm569967.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Drugs are subject to this recall: