Why it was recalled
Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with an incorrect identifier code on the embossed tablets..
Product description
Lisinopril Tablets, USP 10 mg, Rx only, 1000 count bottles, Manufactured for: Mylan Pharmaceuticals Inc ,Morgantown, WV 26505 U.S.A. Made in India; NDC 0378-20740-10
Lot numbers, UPCs & expiration codes
Lot# 3002450; exp 8/14
Where it was sold
Nationwide.
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-269-2013
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- Feb 26, 2013
- FDA report date
- May 1, 2013
- Quantity
- 2,405 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Mylan Pharmaceuticals Inc.
Original FDA data
Every field from FDA enforcement report D-269-2013, exactly as published.
Show all FDA fields
- City
- Morgantown
- State
- WV
- Status
- Terminated
- Country
- United States
- Event ID
- 64924
- Address
- 781 Chestnut Ridge Rd
- Code information
- Lot# 3002450; exp 8/14
- Postal code
- 26505-2730
- Report date
- May 1, 2013
- Product type
- Drugs
- Recall number
- D-269-2013
- Classification
- Class III
- Recalling firm
- Mylan Pharmaceuticals Inc.
- Product quantity
- 2,405 bottles
- Termination date
- Dec 5, 2013
- Reason for recall
- Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with an incorrect identifier code on the embossed tablets..
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Lisinopril Tablets, USP 10 mg, Rx only, 1000 count bottles, Manufactured for: Mylan Pharmaceuticals Inc ,Morgantown, WV 26505 U.S.A. Made in India; NDC 0378-20740-10
- Distribution pattern
- Nationwide.
- Recall initiation date
- Feb 26, 2013
- Initial firm notification
- Letter
- Center classification date
- Apr 23, 2013