Annora Pharma Lacosamide Tablets Recall: Possible Selexipag Mix-Up

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Recalling firmAnnora Pharma Private LimitedSy. No.261, Plot No. 13 And 14, Annaram Village, Gummadidal Mandal, Jinnaram Mandal, Sangareddy District, Medak · Hyderabad, N/A N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Annora Pharma is recalling 100mg Lacosamide tablets that may contain Selexipag 1000mcg tablets. This mix-up could lead to incorrect medication use, especially since these are prescription-only drugs.

Why it’s dangerous

The recall addresses a possible mix-up where Selexipag 1000mcg tablets were mistakenly included in Lacosamide tablets. Selexipag is a different medication with a different dosage and purpose, which could cause incorrect treatment.

Who’s affected

Prescription holders of Lacosamide tablets (100mg, 60-count) from Annora Pharma. Those with specific medical conditions requiring precise dosing are most at risk.

How to tell if you have this one

Check for NDC code 31722-813-60 on the bottle. Look for lot numbers A253999 or A254000. Products were manufactured for Camber Pharmaceuticals in New Jersey and expire September 30, 2027.

Brand
Annora Pharma
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for NDC code 31722-813-60 and lot numbers A253999 or A254000 on the bottle.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

A possible mix-up of Selexipag 1000mcg tablets with Lacosamide tablets was reported, which could lead to incorrect medication use.

What should I do if I have this product?

Check the product details to see if it matches the recalled items. If it does, contact your doctor or pharmacist for guidance.

Is there a deadline to act?

The recall record does not specify a deadline for action.

Take action

Contact Annora Pharma

We’ve drafted a message you can send Annora Pharma to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0626-2026 — Annora Pharma Annora Pharma

Hello,

I own a Annora Pharma that is covered by recall D-0626-2026 from Annora Pharma.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0626-2026 (June 4, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0626-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Annora Pharma Private Limited recalls Lacosamide Tablets, USP, C V, 100mg, Rx only, 60-count bottle, By: Annora Pharma Pvt., Ltd, Sangareddy -502313,

Lower-risk recall