FDA Drug Recalls

Recalls / Class I

Class ID-0452-2024

Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.

Product

Pink Pussycat Honey, net wt: 20gx12 sachets, UPC 7 918750 046557

Affected lot / code info
All Lots

Why it was recalled

Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.

Recalling firm

Firm
Pyramids Wholesale Inc.
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
464 E 4th St, N/A, Los Angeles, California 90013-1604

Distribution

Quantity
149 boxes
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2024-03-19
FDA classified
2024-04-22
Posted by FDA
2024-05-01
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0452-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.