Multi-event February 2017 FDA Recall Zenatane by Dr. Reddy's Laboratories, Inc.

This Multi-event Class III drug recall was voluntarily initiated by Dr. Reddy's Laboratories, Inc. on February 15, 2017 for the product Zenatane. The FDA reported the reason for recall as failed dissolution specifications - low dissolution results at s3 stage.. The product was distributed Nationwide and the recall is currently terminated.

Reported Recall Events

Recall Number: D-0508-2017

Reason for Recall
Failed dissolution specifications - low dissolution results at S3 stage.
Initiated
02-15-2017
Reported
03-08-2017
Quantity
4014 cartons

Recall Profile & Regulatory Data

Class III - is a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Dr. Reddy's Laboratories, Inc.
Zenatane (isotretinoin) capsules, 30 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 5511-113-81

Batch or Lot Expiration Information

Lot# KB60036, Exp 12/17

Recall Number: D-0509-2017

Reason for Recall
Failed dissolution specifications - low dissolution results at S3 stage.
Initiated
02-15-2017
Reported
03-08-2017
Quantity
4404 cartons

Recall Profile & Regulatory Data

Class III - is a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Dr. Reddy's Laboratories, Inc.
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

Batch or Lot Expiration Information

Lot# KB60197, Exp 2/18

Recall Number: D-0507-2017

Reason for Recall
Failed dissolution specifications - low dissolution results at S3 stage.
Initiated
02-15-2017
Reported
03-08-2017
Quantity
12132 cartons

Recall Profile & Regulatory Data

Class III - is a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Dr. Reddy's Laboratories, Inc.
Zenatane (isotretinoin) capsules, 20 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 55111-136-81

Batch or Lot Expiration Information

Lot# KB50877, KB50878, Exp 11/17; KB50878, 01KB60251, Exp 3/18

Recall Number: D-0506-2017

Reason for Recall
Failed dissolution specifications - low dissolution results at S3 stage.
Initiated
02-15-2017
Reported
03-08-2017
Quantity
4032 cartons

Recall Profile & Regulatory Data

Class III - is a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Dr. Reddy's Laboratories, Inc.
Zenatane (isotretinoin) capsules, 40 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 55111-137-81

Batch or Lot Expiration Information

Lot# 01KB60250, Exp 3/18