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Questions about the BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE Bisoprolol Fumarate and Hydrochlorothiazide tablets, USP, 2.5 mg/6.25 mg, 100-co Recall 2026

Answers to common safety, symptoms, and disposal questions for this specific recall.

Key recall facts

  • Brand: BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE
  • Reason: cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
  • Published: 1/21/2026

Is the BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE recall still active?

Yes, this recall is currently active as of January 21, 2026. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: Lot # GBHL24005A, Exp Date: 09/2026. Check the label on your product.

What should I do if I have the recalled BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE?

Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.

Why was BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE recalled in 2026?

cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.