Class II · Moderate risk
Cold/Sinus Pain Reliever/Fever Reducer Nasal Decongestant
cGMP deviations
Is Acetaminophen recalled?
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.
Acetaminophen recalls on record
none so far in 2026; 240 on record, newest first
Class II · Moderate risk
Pain Away Pain Reliever/Fever Reducer
cGMP deviations
Class II · Moderate risk
Headache & Congestion Sinus Relief
cGMP deviations
Class II · Moderate risk
Cold Relief
cGMP deviations
Class II · Moderate risk
Backache & Muscle Relief
cGMP deviations
Class II · Moderate risk
Multi-Symptom Cramp Relief
cGMP deviations
Class II · Moderate risk
Cold Relief Severe Pain/Cough
cGMP deviations
Class II · Moderate risk
Multi Symptom Cold Relief
cGMP deviations
Class II · Moderate risk
Cetafen Non-aspirin pain reliever
cGMP deviations
Class II · Moderate risk
Class II · Moderate risk
Legatrin PM Pain Reliever/Sleep Aid
cGMP deviations
Class II · Moderate risk
Extra Strength
cGMP deviations
Class II · Moderate risk
Chloresin
cGMP deviations
Class II · Moderate risk
Maximum Strength Non Aspirin Pain Reliever/Fever Reducer
cGMP deviations
Class II · Moderate risk
AERO TAB Cold Relief
cGMP deviations
Class II · Moderate risk
Class II · Moderate risk
Extra Strength Headache
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Class II · Moderate risk
Medique Pain-Off
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Class II · Moderate risk
Physicians CARE Extra Strength PAIN RELIEVER
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Class II · Moderate risk
Hydrocodone Bitartrate and Acetaminophen Tablets
Product Mix-up
Class II · Moderate risk
Acetaminophen Oral Suspension
cGMP Deviations: Product manufactured with contaminated raw ingredient.
Class II · Moderate risk
Acetaminophen Oral Suspension
cGMP Deviations: Product manufactured with contaminated raw ingredient.
Class II · Moderate risk
Acetaminophen Child Bubble Gum Flavored Oral Suspension
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Class II · Moderate risk
Acetaminophen Child Bubble Gum Flavored Oral Suspension
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Class II · Moderate risk
Children's Pain & Fever Acetaminophen
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
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