Why it was recalled
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Product description
Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/10 mg, a) 90 count (NDC 43598-742-90) and b) 1000 count (NDC 43598-742-10) bottles, Rx only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA, , packaged in bottles.
Lot numbers, UPCs & expiration codes
a) L100256, exp 01/2023; b) L100257, exp 01/2023
Where it was sold
Nationwide in the US
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0081-2022
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Oct 5, 2021
- FDA report date
- Nov 10, 2021
- Quantity
- a) 776 bottles, b) 84 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Dr. Reddy's Laboratories, Inc.
Original FDA data
Every field from FDA enforcement report D-0081-2022, exactly as published.
Show all FDA fields
- City
- Princeton
- State
- NJ
- Status
- Terminated
- Country
- United States
- Event ID
- 88798
- Address
- 107 College Rd E
- Code information
- a) L100256, exp 01/2023; b) L100257, exp 01/2023
- Postal code
- 08540-6623
- Report date
- Nov 10, 2021
- Product type
- Drugs
- Recall number
- D-0081-2022
- Classification
- Class II
- Recalling firm
- Dr. Reddy's Laboratories, Inc.
- Product quantity
- a) 776 bottles, b) 84 bottles
- Termination date
- Feb 16, 2023
- Reason for recall
- Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/10 mg, a) 90 count (NDC 43598-742-90) and b) 1000 count (NDC 43598-742-10) bottles, Rx only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA, , packaged in bottles.
- Distribution pattern
- Nationwide in the US
- Recall initiation date
- Oct 5, 2021
- Initial firm notification
- Letter
- Center classification date
- Oct 29, 2021