The National Health Surveillance Agency (Anvisa) published in the Official Gazette on Thursday, 23, a resolution requesting the suspension and recall of 19 lots of the drug Tylenol Gotas 200mg / ml Oral Solution.
This determination was made after Anvisa identified problems in the dripping of the bottles. The dripper may come off of the product by pressing the bottle, which may lead to an accidental overdose of the product.
The Janssen-Cilag Pharmaceutical Laboratory, maker of the drug, has announced that it will collect all 19 batches of the drug, manufactured between December 2011 and November 2012, exceeding three million units collected.
The recall campaign will start next Monday, the 27th. The lots that will be collected are: PPL055, PPL056, PPL057, RAL030, RCL088, RFL095, RLF096, RGL052, RKL037, RLL015, RLL087, RML007, RML135, RML135 , RML175, RNL049, REL036 and RJL123.
If you have the product at home, do not use directly in the mouth, always use a dosage spoon.
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