The Perrigo Company is voluntarily recalling two batches of its children’s Guaifenesin grape liquid (100mg/5 mL) and three batches of its children's Guaifenesin DM cherry liquid (100mg guaifenesin and 5mg dextromethorphan HBr/ 5 ml) after a dosing cup with the wrong markings was included with the 4 oz. bottles. The medications are sold at nine major stores under different brand names across the country. (See below for a full list)

The U.S. Food and Drug Administration (FDA) is aware of the recall. A company statement says that using these recalled products “according to labeled instructions with an affected dosing cup is unlikely to result in serious side effects”, and it says that there have been no reports of anyone becoming sick.

"There have been no reports of adverse events to Perrigo as a result of the incorrect dosage markings," Perrigo's Chairman and CEO Joseph C. Papa said in a statement. "Perrigo is taking this action to maintain the highest possible product quality standards for our retail customers and consumers. We are taking this action because it is the right thing to do."

Recalled lots, along with their corresponding branded labels, are listed below:

GUAIFENESIN GRAPE LIQ 4 OZ

STORE LOT
NUMBER
EXPIRATION
DATE
H.E.B 5LK0592 08/2017
CVS 5MK0340 5MK0340

GUAIFENESIN DM CHRY LIQ 4 OZ

 STORE  LOT
NUMBER
EXPIRATION DATE 
 Sunmark  5LK0528, 5LK0630   03/2017
 Rite-Aid   5LK0528, 5LK0630  03/2017
 Topcare  5LK0528, 5LK0630, 5LK0779   03/2017
 Kroger  5LK0528, 5LK0630   03/2017
 GoodSense   5LK0528   03/2017
 Dollar General   5LK0630   03/2017
 Care One   5LK0630   03/2017
 CVS  5LK0630   03/2017

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