Dr. Reddy's Bortezomib Vials: Failed Stability Specifications

Take action

Contact the company & request your remedy

Recalling firmDr. Reddy's Laboratories, Inc.107 College Rd E · Princeton, NJ 08540-6623

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Dr. Reddy's is recalling certain Bortezomib vials because they failed stability tests. This could mean the medication might not be safe or effective once opened. Patients using these vials should contact their doctor or pharmacy for guidance.

Why it’s dangerous

The vials failed stability specifications, meaning the medication may degrade over time. This could lead to reduced effectiveness or potential safety issues if the vial is not stored properly.

Who’s affected

Patients prescribed Bortezomib by a doctor who use the recalled vials. Those with specific medical conditions requiring this medication are most at risk.

How to tell if you have this one

Check for NDC 43598-865-60 and lot number H210233 on the vial. The vials were manufactured in India by Dr. Reddy's Laboratories Limited in Visakhapatnam.

Brand
Dr. Reddy's
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Vial Details
Look for NDC 43598-865-60 and lot number H210233 on the vial.

✎ GovInfoNow

Questions people ask

Is this recall affecting my medication?

This recall applies to specific vials with NDC 43598-865-60 and lot number H210233. If you have these, contact your doctor or pharmacy.

What should I do if I have the recalled vial?

The recall does not specify a remedy, so contact your doctor or pharmacy for guidance.

How can I check if my vial is affected?

Check for NDC 43598-865-60 and lot number H210233 on the vial. The vials were manufactured in India by Dr. Reddy's Laboratories Limited in Visakhapatnam.

Take action

Contact Dr. Reddy's

We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0577-2022 — Dr. Reddy's Dr. Reddy's

Hello,

I own a Dr. Reddy's that is covered by recall D-0577-2022 from Dr. Reddy's.

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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-0577-2022 (January 19, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0577-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.

Dr. Reddy's Laboratories, Inc. recalls Bortezomib, 3.5 mg/vial, Single-Dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046,

Lower-risk recall