Teva Parenteral Medicines Initiates Voluntary Nationwide Recall of Select Lots of Adrucil® (fluorouracil Injection, Usp) 5 G/100 Ml (50 Mg/ml) Due to Particulate Matter

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Title: Teva Parenteral Medicines Initiates Voluntary Nationwide Recall of Select Lots of Adrucil® (fluorouracil Injection, Usp) 5 G/100 Ml (50 Mg/ml) Due to Particulate Matter

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Teva Parenteral Medicines Initiates Voluntary Nationwide Recall of Select Lots of Adrucil® (fluorouracil Injection, Usp) 5 G/100 Ml (50 Mg/ml) Due to Particulate Matter

05/04/2015 09:34 PM EDT

Teva Parenteral Medicines today announced a voluntary recall of eight lots of Adrucil® (fluorouracil injection, USP) 5 g/100 mL (50 mg/mL) due to the potential presence of particulate matter identified as aggregate of silicone rubber pieces from a filler diaphragm and fluorouracil crystals.

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