PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: July 20, 2016 Initiated: June 28, 2016 #D-1255-2016

Product Description

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

Reason for Recall

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

Details

Units Affected
2077 bottles
Distribution
Nationwide. No foreign distribution.
Location
Camarillo, CA

Frequently Asked Questions

What product was recalled?
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. Recalled by Golden State Medical Supply Inc.. Units affected: 2077 bottles.
Why was this product recalled?
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
Which agency issued this recall?
This recall was issued by the FDA Drug on July 20, 2016. Severity: Low. Recall number: D-1255-2016.