RecallRadar
ModerateReported March 11, 2026

Product label: Temozolomide Capsules, 5mg

Recalled by Rising Pharma Holding, Inc.

Product image for Product label: Temozolomide Capsules, 5mg, packaged in 5-capsule bottles, Rx only, Manufactured for: Rising Pharmaceuticals, Inc., Allendale, NJ 07401, Country of origin: Taiwan, NDC 16571-816-51.
Product image via DailyMed (National Library of Medicine). It may show general packaging and not the exact recalled lot — always confirm using the codes below.

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Rising Pharma Holding, Inc. has recalled Product label: Temozolomide Capsules, 5mg, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on March 11, 2026 and was initiated on March 3, 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 Product label: Temozolomide Capsules, 5mg, with approximately 1200 bottles affected. The company behind the recall is Rising Pharma Holding, Inc., based in East Brunswick, NJ. The FDA describes the product as: “Product label: Temozolomide Capsules, 5mg, packaged in 5-capsule bottles, Rx only, Manufactured for: Rising Pharmaceuticals, Inc., Allendale, NJ 07401, Country of origin: Taiwan, NDC 16571-816-51.”

Why was Product label: Temozolomide Capsules, 5mg recalled?

According to the FDA, the stated reason for the recall is: “Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-month long term stability testing.” 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 Product label: Temozolomide Capsules, 5mg, compare it against the product description and identifying codes (Lot #: 1TM0524003A, Exp. Date 09/2026.) 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 Rising Pharma Holding, Inc. 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.

Full recall details

Status
Ongoing
Date reported
March 11, 2026
Recall started
March 3, 2026
Distributed in
NJ
What was recalled
Product label: Temozolomide Capsules, 5mg, packaged in 5-capsule bottles, Rx only, Manufactured for: Rising Pharmaceuticals, Inc., Allendale, NJ 07401, Country of origin: Taiwan, NDC 16571-816-51.
Why it was recalled (as stated by the FDA)
Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-month long term stability testing
How to identify the affected product
Lot #: 1TM0524003A, Exp. Date 09/2026.
Amount recalled
1200 bottles

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 Product label: Temozolomide Capsules, 5mg recalled?+

According to the FDA: Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-…

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 Product label: Temozolomide Capsules, 5mg?+

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.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: D-0384-2026. Information last synced from the FDA on July 6, 2026.