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FDA (Drug enforcement)Recalled 2017-05-22closedclass ii

Dr. Reddy's Laboratories, Inc.: Zenatane (isotretinoin) Capsules, USP, 30 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured By: Cipla Limited, Kurkumbh Village, Pune 413802 In

Is my product affected?

Zenatane (isotretinoin) Capsules, USP, 30 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured By: Cipla Limited, Kurkumbh Village, Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-113-81

  • Brand ZENATANE

Check against the official notice below — it lists the full affected range.

What happened

Dr. Reddy's Laboratories, Inc. is recalling Zenatane (isotretinoin) 30 mg capsules in 30-count prescription packs distributed nationwide in the USA and Puerto Rico. The recall affects 223,650 cartons due to failed dissolution specifications, meaning the capsules did not dissolve properly according to required standards. The recalled lots span multiple expiration dates from May 2017 through August 2018, with lot numbers beginning with KB50, KB60, 01KB60, and 79KB60 designations.

The source document does not specify a remedy or recommended action for consumers who possess this product.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Failed Dissolution Specifications: out of specification results observed for low dissolution.

Details from the source

Reason for recall: Failed Dissolution Specifications: out of specification results observed for low dissolution. Distribution: Nationwide in the USA and Puerto Rico Quantity: 223,650 cartons Lot/code info: Lot #: KB50414, KB50456, Exp 05/17; KB50457, KB50458, KB50459, KB50460, Exp 06/17; KB50580, KB50581, KB50582, KB50583, KB50599, KB50600, Exp 07/17; KB50646, KB50647, KB50721, KB50722, KB50723, KB50724, Exp 09/17; KB50833, KB50834, KB50835, KB50836, KB50837, Exp 10/17; KB50902, KB50903, KB50904, Exp 11/17; KB60037, KB60038, KB60039, KB60040, KB60041, Exp 12/17; KB60109, KB60110, KB60111, KB60112, KB60113, Exp 01/18; 01KB60249, 01KB60266, 01KB60268, 01KB60269, 01KB60284, Exp 03/18; 01KB60369, 01KB60372, 79KB60368, 79KB60371, Exp 05/18; 79KB60507, 79KB60508, 79KB60509, 79KB60510, 79KB60511, 79KB60512, 79KB60513, 79KB60514, 79KB60515, 79KB60516, Exp 07/18; 79KB60570, 79KB60571, 79KB60585, 79KB60586, Exp 08/18;

Source

Official record: FDA (Drug enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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