Lisinopril Tablets recall: Labeling Error
Lisinopril Tablets, USP, 30 mg, Rx only, 100 tablets, NDC 65862-041-01 Manufactured for: Aurobindo Pharma USA Inc. 2400 Route 130 North, Dayton, NJ…
Why was Lisinopril Tablets recalled?
Labeling: Label Error on Declared Strength: Incorrect strength on side display panel of label
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot KP3012001-A Exp.12/13 Lot KP3012002-A Exp.12/13
- Product
- Lisinopril Tablets, USP, 30 mg, Rx only, 100 tablets, NDC 65862-041-01 Manufactured for: Aurobindo Pharma USA Inc. 2400 Route 130 North, Dayton, NJ…
- Recalling firm
- Aurobindo Pharma USA Inc
- Quantity
- 1776 bottles
- Distribution
- Nationwide
- Recall date
- June 5, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)