Ascend Laboratories recalls 90-tablet Ibuprofen and Famotidine tablets (Rx only) due to a stray Rasagiline Mesylate tablet found in unopened bottles. No remedy provided in official notice.
Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet was discovered in an unopened bottle of Ibuprofen and Famotidine.
Ascend Laboratories is recalling Ibuprofen and Famotidine tablets (800mg/26.6mg) that may contain a stray Rasagiline Mesylate tablet. This could pose a risk if taken, as Rasagiline Mesylate is a medication that may cause adverse effects when ingested.
The recall involves a stray Rasagiline Mesylate tablet found in unopened bottles of Ibuprofen and Famotidine. Rasagiline Mesylate is a medication that could cause adverse effects if taken, potentially leading to health issues.
People who have purchased these specific tablets from Ascend Laboratories in the U.S. are affected. Those with medical conditions requiring these medications are at higher risk if they consume the stray tablet.
Check for the product name 'Ibuprofen and Famotidine Tablets 800mg/26.6mg, Rx Only, 90 Tablets per Bottle' with NDC 67877-626-90 or 23140190. These were manufactured by Alkem Laboratories in India and distributed by Ascend Laboratories in New Jersey.
Look for the NDC numbers 67877-626-90 or 23140190 on the packaging to confirm if the product is recalled.
The recall states a stray Rasagiline Mesylate tablet was found in unopened bottles. Rasagiline Mesylate is a medication that could cause adverse effects if taken, but the official notice does not specify the exact risk level.
Check for the product name 'Ibuprofen and Famotidine Tablets 800mg/26.6mg, Rx Only, 90 Tablets per Bottle' with NDC numbers 67877-626-90 or 23140190.
The official recall notice does not provide a remedy, so no specific action is required beyond checking the product details.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0237-2024 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0237-2024 from Ascend Laboratories. 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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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.
