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FDAFDA · Food and drugs·Recall number D-1255-2016

DULOXETINE Delayed-Release Capsules, USP, 60 mg, 1000 count bottles, Rx only, Manufactured by: Laboratorios del Dr. Esteve, SA, Martorelles, Barcelona --- NDC 60429-166-10

Published July 20, 2016 · Recall initiated: June 28, 2016

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

Labeling; Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on container label is 02/2019, correct expiration date should be 02/2018

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
DULOXETINE
Manufacturer
Golden State Medical Supply Inc.
Distributor
Nationwide. No foreign distribution.
Lot
Lot# GS011709, GS012352
Risk classification
Class III
Area (FDA)
drug
Country
United States

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