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FDAFDA · Food and drugs·Recall number D-0519-2017

Clindamycin Phosphate Topical Solution USP, 1%, packaged in a) 30 mL applicator bottles (NDC 0472-0987-91) and b) 60 mL applicator bottles (NDC 0472-0987-92), Rx Only, Manufactured by: G&W Laboratories, Inc., 111 Coolidge Street, South Plainfield, NJ 07080; Distributed by: Actavis Mid Atlantic LLC, 1877 Kawai Road, Lincolnton, NC 28092.

Published March 22, 2017 · Recall initiated: February 28, 2017

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

CGMP Deviations: an expired active ingredient was used in the manufacture of these recalled lots.

What to do

Voluntary: Firm initiated · E-Mail

Recall details

Manufacturer
G & W Laboratories, Inc.
Distributor
Nationwide in the USA.
Lot
Lot #'s: a) 032100042, 032100043, 032100044, 032100045, Exp 06/17; b) 032100038, 032100039, 032100040, 032100041, Exp 05/17; 032100046, 032100047, 032100048, 032100049, Exp 06/17.
Risk classification
Class III
Area (FDA)
drug
Country
United States

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