FDA Drug Recalls

Recalls / Class II

Class IID-0538-2022

Product

HPC Tablet (Acetaminophen 110 mg, Aspirin 162 mg, Caffeine 32.4 mg, Salicylamide 152 mg) Bulk Container, ULTRAtab Laboratories, Inc., Highland, NY NDC 62969-242-00

Affected lot / code info
Product Codes: L242SRC Bulk Lot: 18K086, 18L009, 18L050, 18L083, 18M025, 18M073, 18M098, 19A010, 19A084, 19A105, 19A107; Product Code: L242L Bulk Lot: 19H014; Product Code: L242PA Bulk Lot: 18F072, 18L119, 19A067, 19G043; Product Code: L242N Bulk Lot: 19H040

Why it was recalled

CGMP Deviations

Recalling firm

Firm
ULTRAtab Laboratories, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
50 Toc Dr, N/A, Highland, New York 12528-1506

Distribution

Quantity
50,585,623 tablets
Distribution pattern
Bulk product was distributed to 3 distributors who may have distributed finished product.

Timeline

Recall initiated
2022-01-26
FDA classified
2022-02-09
Posted by FDA
2022-02-16
Terminated
2025-01-07
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0538-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.