FDA Drug Recalls

Recalls / Class II

Class IID-1367-2019

Product

Kid Kare Childrens Cough/Cold Liquid, Antihistamine, Cough Suppressant, Nasal Decongestant, Cherry Flavored, Alcohol Free, (Chlorpheniramine Maleate, USP 2 mg, Dextromethorphan HBr, USP 10 mg, Pseudoephedrine HCl, USP 30 mg in each 2 tsp (10mL)), 4 Fl. oz. bottle, NDC: 0536-2310-97, Distributed by Rugby Laboratories, Livonia MI 48152.

Affected lot / code info
Lot #s: 17E009, Exp. 05/2019; 17L004; 17L004A, 17L020, Exp. 11/2019; 17M029, Exp. 12/2019; 18C010; 18C025, Exp. 03/2020; 18J020, Exp. 09/2020.

Why it was recalled

cGMP Deviations: Potential product contamination with Burkholderia cepacia (B.cepacia) and Ralstonia pickettii (R. pickettii).

Recalling firm

Firm
Torrent Pharma Inc
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
2091 Hartel Ave, N/A, Levittown, Pennsylvania 19057-4506

Distribution

Quantity
66,060 bottles
Distribution pattern
Product was distributed to 9 distributors, direct accounts and relabelers who may have further distributed the product throughout the United States.

Timeline

Recall initiated
2019-05-21
FDA classified
2019-06-13
Posted by FDA
2019-06-19
Terminated
2020-10-06
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1367-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.