FDA Drug Recalls

Recalls / Class II

Class IID-0862-2021

Product

Cedar Fever Drops, 20% USP ALCOHOL, 30 mL, homeopathic drug for symptoms of cder allerges, Manufactured for Peoples RX, 3801 S Lamar, Austin, TX 78704. UPC 7 40640 64166 8

Affected lot / code info
Lot # 25586, 27410

Why it was recalled

Out-of-specification test results obtained for identification testing based on HPTLC analysis.

Recalling firm

Firm
Washington Homeopathic Products, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
260 J R Hawvermale Way, N/A, Berkeley Springs, West Virginia 25411-6957

Distribution

Quantity
1,931 bottles
Distribution pattern
Distributed Nationwide in the USA

Timeline

Recall initiated
2021-08-20
FDA classified
2021-09-29
Posted by FDA
2021-10-06
Terminated
2022-06-21
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0862-2021. 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