Zenatane recall: Failed Dissolution
Zenatane (isotretinoin) capsules, 10 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-135-81
Why was Zenatane recalled?
Failed dissolution specifications - low dissolution results at S3 stage.
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 # KB60197, Exp 2/18
- Product
- Zenatane (isotretinoin) capsules, 10 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-135-81
- Recalling firm
- Dr. Reddy's Laboratories, Inc.
- Quantity
- 4404 cartons
- Distribution
- U.S. Nationwide
- Recall date
- March 8, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)