FDA Drug Recalls

Recalls / Class II

Class IID-0466-2022

Product

AERO TAB Cold Relief (acetaminophen 325 mg, Guaifenesin 200mg, Phenylephrine HCl 5mg) 2 tablet packets, Mfg. for: Aero Healthcare, Valley Cottage, NY 10989

Affected lot / code info
Lot #: AK9565, Exp. Date 04/2022

Why it was recalled

cGMP deviations

Recalling firm

Firm
Ultra Seal Corporation
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
521 Main St, N/A, New Paltz, New York 12561-1609

Distribution

Quantity
226,390 packets
Distribution pattern
Nationwide within the United States

Timeline

Recall initiated
2022-01-24
FDA classified
2022-01-31
Posted by FDA
2022-02-09
Terminated
2023-10-16
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0466-2022. 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