The recall was issued by the Perrigo Company because of "incorrect dose markings" on some dosage cups.

Ill woman at home
Piotr Marcinski-Thinkstock
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Perrigo wants everyone to be aware that "use of these products according to labeled instructions with an affected dosing cup is unlikely to result in serious side effects, and no reports related to overdose have been received to date". 

initiated a voluntary product recall in the US to the retail level of 2 batches of its children's guaifenesin grape liquid (100mg/5 mL) and 3 batches of its children's guaifenesin DM cherry liquid (100mg guaifenesin and 5mg dextromethorphan HBr/ 5 ml) sold in 4 oz. bottles with dosage cup in a box under the store brand products listed below.

GUAIFENESIN GRAPE LIQ 4 OZ

Label

Lot number

Expiry

H.E.B

5LK0592

08/2017

CVS

5MK0340

08/2017

 

GUAIFENESIN DM CHRY LIQ 4 OZ

Label

Lot number

Expiry

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

If you have any questions, you are asked to contact your physician or healthcare provider, or if they or your children experience any problem that could possibly be related to this drug product.

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