Home / Recalls / Allergan Sales, LLC / D-1064-2016

D-1064-2016 Class II Terminated

Recalled by Allergan Sales, LLC — Waco, TX

FDA drug recall D-1064-2016 was initiated by Allergan Sales, LLC on May 10, 2016 and is designated Class II. Reason for recall: Failed Content Uniformity Specifications. The recall status is terminated (terminated Dec 6, 2017). Affected quantity: 17802 units.

Recall details

Product Type: Drugs
Report Date: Jul 13, 2016
Initiation Date: May 10, 2016
Termination Date: Dec 6, 2017
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 17802 units

Product description

Tazorac (tazarotene) Gel 0.05%, Rx only, packaged in a) 30g (NDC 0023-8335-03) and b) 100g (NDC 0023-8335-10) tubes, Allergan Inc, Irvine, CA 92612

Reason for recall

Failed Content Uniformity Specifications.

Distribution pattern

Nationwide and Puerto Rico

Code information

Lot #: a) 84172, b) 84173, Exp FEB/2017

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-1064-2016
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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