FDA Drug Recalls

Recalls / Class II

Class IID-0528-2022

Product

Coated APAP 325 mg Phenyl HCl 5 mg tablet (Acetaminophen 325 mg, Phenylephrine HCl 5mg) Bulk Container, ULTRAtab Laboratories, Inc., Highland, NY NDC 62959-134-00

Affected lot / code info
Product Codes: C134LC Bulk Lots: 18K055 18M081 19A097 19B024 19C054 19E092 19G094 19J042

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
14,566,510 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-0528-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.