Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP
Recalled by Glenmark Pharmaceuticals Inc., USA
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Glenmark Pharmaceuticals Inc., USA has recalled Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on June 24, 2026 and was initiated on May 27, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP. The company behind the recall is Glenmark Pharmaceuticals Inc., USA, based in Elmwood Park, NJ. The FDA describes the product as: “Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP, 0.5mg/0.035mg, 0.75mg/0.035mg, 1 mg/0.0.35mg, 3 Blister Cards each containing 28 tablets, 28 day regimen, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd., Colvale-Bardez, Goa 403 513, Ind…”
Why was Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP recalled?
According to the FDA, the stated reason for the recall is: “Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.” In plain terms, this recall relates to a chemical impurity.
This recall involves an unwanted chemical detected in the medicine — often a nitrosamine impurity, which regulators limit because long-term exposure above set levels may increase health risks. Regulators recall affected batches as a precaution. Health authorities generally advise talking to a doctor or pharmacist before stopping a prescribed medicine.
What should you do?
If you think you may have bought Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP, compare it against the product description and identifying codes (Lot #: 20240411, Exp: 6/30/2026; 20250252, Exp: 3/31/2027) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Glenmark Pharmaceuticals Inc., USA or your local health authority.
About this recall
This recall was distributed in NJ. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Who this recall affects
This recall matters to anyone who bought Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP. Even if you feel fine, it's worth checking what you have on hand rather than assuming you were missed.
Distribution listed in the notice: USA Nationwide..
What chemical impurity actually means
This recall involves an unwanted chemical detected in the medicine — often a nitrosamine impurity, which regulators limit because long-term exposure above set levels may increase health risks. Regulators recall affected batches as a precaution. Health authorities generally advise talking to a doctor or pharmacist before stopping a prescribed medicine.
In this case, the concern applies specifically to Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP from Glenmark Pharmaceuticals Inc., USA — not to the wider category of products. Similar items from other brands aren't part of this recall.
How to check whether you have it
On medicine bottles, the lot number and expiration date are printed on the pharmacy label or stamped directly on the manufacturer's bottle — often near the bottom edge or on the back. If a pharmacy label covers it, your pharmacist can look up the lot they dispensed.
Compare what you find against the identifying details in this recall: Lot #: 20240411, Exp: 6/30/2026; 20250252, Exp: 3/31/2027
What to do if you already bought it
Do not stop taking a prescribed medicine on your own because of a recall — for many conditions, an interrupted dose carries its own risk.
Instead, check the lot number against the details above and contact your pharmacist, who can confirm what they dispensed and arrange a replacement.
If you've had an unexpected reaction, contact your healthcare provider. Problems can also be reported to the FDA's MedWatch program.
Full recall details
- Status
- Ongoing
- Date reported
- June 24, 2026
- Recall started
- May 27, 2026
- Distributed in
- NJ
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP recalled?+
According to the FDA: Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specif…
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: D-0588-2026. Information last synced from the FDA on August 20, 2026.
