FDA Drug Recalls

Recalls / Class II

Class IID-0276-2019

Product

Children's 24 Hour Allergy (cetirizine hydrochloride) Oral Solution 1 mg/mL, Bubble Gum Flavor, Sugar Free/Dye Free, 4 FL OZ (120 mL) bottle, Dist. by Meijer Distribution, Inc., Grand Rapids, MI 40644, NDC 41250-106-08, UPC 7 13733 88578 2.

Affected lot / code info
Lot # 313342, Exp 12/18

Why it was recalled

Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.

Recalling firm

Firm
Taro Pharmaceuticals U.S.A., Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
3 Skyline Dr, Hawthorne, New York 10532-2174

Distribution

Quantity
12,432 bottles
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2018-10-19
FDA classified
2018-11-20
Posted by FDA
2018-11-21
Terminated
2020-11-03
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0276-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls