Metformin Hydrochloride Extended-Release Tablets 1000mg recall
FDA recall D-0328-2025 · initiated Mar 13, 2025
Glenmark Pharmaceuticals Inc., USA recalled Metformin Hydrochloride Extended-Release Tablets 1000mg in Mar 2025 — an FDA Class II recall (D-0328-2025) because CGMP Deviations.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
CGMP Deviations
The manufacturing process itself
The FDA found the process itself out of compliance, usually before any defective product was identified.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: N/A
Details
- Product
- Metformin Hydrochloride Extended-Release Tablets 1000mg, 90-count bottle. Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc. USA, Mahwah, NJ 07430. NDC 68462-521-90.
- Recalling company
- Glenmark Pharms
- Classification
- Class II
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- U.S. Nationwide
- Initiated
- Mar 13, 2025
- FDA report date
- Apr 16, 2025
Frequently asked
- Was Metformin Hydrochloride Extended-Release Tablets 1000mg recalled?
- Glenmark Pharmaceuticals Inc., USA recalled Metformin Hydrochloride Extended-Release Tablets 1000mg in Mar 2025 — an FDA Class II recall (D-0328-2025) because CGMP Deviations. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was Metformin Hydrochloride Extended-Release Tablets 1000mg recalled?
- Per the FDA enforcement record, the reason for recall D-0328-2025 was: CGMP Deviations
- Is a recalled Metformin Hydrochloride Extended-Release Tablets 1000mg dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of Metformin Hydrochloride Extended-Release Tablets 1000mg are affected?
- Distributed: U.S. Nationwide. The recall covers these lots — Lot # 17232088, exp. date Sep-25 17232093, exp. date Sep-25. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0328-2025.