Dr. Reddy's Ezetimibe and Simvastatin Tablets (10mg/20mg) with NDC 43598-744-30 or 43598-744-90 are recalled due to failed excipient specifications. This could affect medication safety. Contact Dr. Reddy's for details.
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Dr. Reddy's Ezetimibe and Simvastatin Tablets (10 mg/20 mg) with specific packaging are being recalled because the manufacturing process used an excipient that failed quality tests. This could potentially affect the safety and effectiveness of the medication.
The tablets were manufactured using an excipient (a substance that helps the drug mix) that failed quality tests for conductivity. This could mean the medication might not work as intended or could cause safety issues.
People who have received the recalled tablets (NDC 43598-744-30 or 43598-744-90) from pharmacies or doctors. Those taking cholesterol-lowering medication are most at risk.
Check for the product name 'Ezetimibe and Simvastatin Tablets, 10 mg/20 mg' with either NDC 43598-744-30 (30-count) or NDC 43598-744-90 (90-count). These are prescription-only medications.
Look for the NDC codes 43598-744-30 or 43598-744-90 on the packaging to confirm if your tablets are recalled.
The recall is due to failed excipient specifications, which could affect medication safety. Do not take these tablets until you confirm they are not recalled.
Check the NDC codes on the packaging: 43598-744-30 (30-count) or 43598-744-90 (90-count). These are prescription-only tablets.
The recall does not specify a remedy, so contact Dr. Reddy's Laboratories for further instructions.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0082-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0082-2022 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.
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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.
