Dr. Reddy's Ezetimibe and Simvastatin 10mg/40mg tablets (30 or 90 count) recalled due to excipient conductivity issues. Rx-only product with NDC codes 43598-743-30 and 43598-743-90. No remedy specified in official recall.
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Dr. Reddy's Ezetimibe and Simvastatin Tablets (10 mg/40 mg) are being recalled because the manufacturing process used an excipient that failed conductivity tests. This could potentially affect the medication's safety and effectiveness, though the recall does not specify a remedy.
The tablets were manufactured using an excipient that failed conductivity tests. This could mean the medication might not work as intended or could cause unexpected reactions in some users. However, the recall does not specify how this affects safety.
People with prescriptions for these specific tablets are affected. Those using the medication as directed without proper medical supervision are at risk due to the excipient issue.
Check for bottles labeled 'Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg' with NDC codes 43598-743-30 (30 count) or 43598-743-90 (90 count). These are prescription-only products with expiration dates of December 2022.
Identify if your prescription contains the specific NDC codes 43598-743-30 or 43598-743-90 for the 30-count or 90-count tablets.
The recall is due to failed excipient specifications, meaning the manufacturing process used an excipient that did not meet conductivity standards.
The official recall does not specify any remedy or action for consumers.
The tablets have expiration dates of December 2022 (as indicated by lot numbers L100158 and L100159).
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-0084-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0084-2022 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.
