Class II · Moderate risk
Torsemide Tablets
CGMP Deviations
Is Torsemide recalled?
Not under an active recall.
Torsemide was recalled 4 times in the past — all now closed. Most recent: Dec 14, 2016.
Most common reason: cGMP deviation (2 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Torsemide. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Torsemide recalls on record
none so far in 2026; 4 on record, newest first
Class II · Moderate risk
Torsemide Tablets
CGMP Deviations
Class II · Moderate risk
TORSEMIDE Tablet
Labeling: Label Mixup; TORSEMIDE, Tablet, 10 mg may be potentially mislabeled as PYRIDOXINE HCL, Tablet, 50 mg, NDC 00536440801, Pedigree: AD30197_22, EXP: 5/9/2014.
Class II · Moderate risk
TORSEMIDE Tablet
Labeling: Label Mixup; TORSEMIDE Tablet, 10 mg may be potentially mislabeled as MEXILETINE HCL, Capsule, 200 mg, NDC 00093874001, Pedigree: AD25264_7, EXP: 5/3/2014.
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