PECGEN DMX Cough Syrup Recall [US]

PECGEN DMX Cough Syrup Recall [US]

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US FlagUS/Silver Spring: NOVIS PR LLC, a Rio Piedras, Puerto Rico establishment, recalls an estimated five (5) batch/lots of PECGEN DMX Cough Syrup due to suspected incorrect dosage information on its label and consequential risk of overdose producing seizures, coma and death, all serious health hazards.

FDA: http://ht.ly/XSof30oRByQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/novis-pr-llc-issues-voluntary-nationwide-recall-pecgen-dmx-due-labeling-error

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

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DG/Health Naturals Baby Cough Syrup Recall [US]

DG/Health Naturals Baby Cough Syrup Recall [US]

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US FlagUS/Silver Spring: Kingston Pharma, LLC, a Massena, New York establishment, recalls certain batch/lots of DG/Health Naturals Baby Cough Syrup + Mucus due to suspected risk of Bacillus Cereus / Bacillus Circulans contamination and consequential risk of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/bvsE30o7Z2E

Direct link: https://www.fda.gov/Safety/Recalls/ucm634052.htm

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

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Ranier’s Rx Labs Compounded Drug Recall [US]

US FlagUS/Silver Spring: Ranier’s Rx Labs Compounded Drug Recall [US]Ranier’s Rx Laboratory, a Jeannette, Pennsylvania establishment, recalls all Sterile Compounded Drug products within expiry to the hospital and consumer level due to suspected non-sterility and possibly contamination with consequential risk of patient hospitalization, significant morbidity, organ damage or fatal outcomes, all serious health and safety hazards.

FDA: http://ht.ly/tIzh30lbJPg

Direct link: https://www.fda.gov/Safety/Recalls/ucm615054.htm

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

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