Theraflu Cold and Flu
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Yes — there is an active recall. 24 ongoing FDA recalls mention Acetaminophen (240 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Acetaminophen. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Defective container: products are packaged in pouches which may not have been fully sealed
Defective container: products are packaged in pouches which may not have been fully sealed
Defective container: products are packaged in pouches which may not have been fully sealed
Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing
Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing
Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina Liquid are being recalled because the product labels are misleading because they may be confused with Pentrexyl, a prescription antibiotic used to treat respiratory illnesses in Mexico.
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