Recall Of Lots Of Diocto Liquid And Diocto Syrup
The National Agency for Food and Drug Administration and Control have been informed that the Rugby Laboratories of Livonia MI, on 3rd August, 2017 recalled lots of Diocto Liquid and Diocto Syrup, (docusate sodium solutions) manufactured by Pharma Tech, LLC of Davie, FL, due to risk of product contamination with Burkholderiacepacia. The use of products […]
Recall Of Man Of Steel 1 And 2
The National Agency for Food and Drug Administration and Control has been informed that the Hungarian Institute of Pharmacy and Nutrition (OGYEI), on 8th August, 2017 revealed that U.S. Food and Drug Administration (FDA), issued a voluntary nationwide recall of Man of Steel 1 and Man of Steel 2 to the consumer level, due to […]
Mislabeled Whole Foods Market Pb& J Parfait
The National Agency for Food and Drug Administration and Control have been informed that the Sunneen Health Foods in Pennsylvania, in collaboration with the U.S. Food and Drug Administration (FDA), on 12th July 2017, recalled mislabelled Whole Foods Market PB & J parfaits due to presence of Soy and tree nuts (almonds and coconut) allergens […]
Recall Of Vancomycin Hydrochloride For Injection
The National Agency for Food and Drug Administration and Control has been informed by the U.S Food and Drug Administration (FDA), that Hospira voluntarily recalled one lot of Vancomycin Hydrochloride for injection, USP, 750mg/vial to the hospital/ retailer level. The recall was due to a confirmed customer report for the presence of particulate matter, confirmed […]
