FDA Drug Recalls

Recalls / Class II

Class IID-1494-2022

Product

CORRECTDOSE Children's COUGH & CHEST CONGESTION DM (Guaifenesin 100 mg / Dextromethorphan 5 mg per 5 mL) 2.04FL. OZ (60mL), packaged in 12-5 individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-321-05 UPC 8 60003 67146 7

Affected lot / code info
Lot # 21014A, EXP Feb. 2023

Why it was recalled

CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.

Recalling firm

Firm
Plastikon Healthcare LLC
Notification channel
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type
Voluntary: Firm initiated
Address
3780 Greenway Cir, N/A, Lawrence, Kansas 66046-5440

Distribution

Quantity
1,464 ampoules
Distribution pattern
Distributed Nationwide in the USA

Timeline

Recall initiated
2022-06-07
FDA classified
2022-09-06
Posted by FDA
2022-09-14
Terminated
2025-06-25
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1494-2022. 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