FlaggedRx← Medication recall checkHome
Class III · Lower riskRecall completed

Duloxetine

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot# GS011709, GS012352
Where it was soldNationwide. No foreign distribution.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byLaboratorios del Dr. Esteve, SA, Martorelles, Barcelona ---
Brand nameDULOXETINE
Generic nameDULOXETINE HYDROCHLORIDE
Active ingredient(s)DULOXETINE HYDROCHLORIDE
Distributed by / forGolden State Medical Supply Inc.
NDC60429-166-10
Show the full FDA record
Full product labelDULOXETINE Delayed-Release Capsules, USP, 60 mg, 1000 count bottles, Rx only, Manufactured by: Laboratorios del Dr. Esteve, SA, Martorelles, Barcelona --- NDC 60429-166-10
Recalling firmGolden State Medical Supply Inc.
DistributionNationwide. No foreign distribution.
Quantity2077 bottles
Recall initiated2016-06-28
Report date2016-07-20
Recall completed2016-11-28
Recall numberD-1255-2016
ClassificationClass III
FDA statusTerminated
Origin on fileCamarillo CA United States

Related

Duloxetine recallsRecent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.