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
- Recalling Firm
- Golden State Medical Supply Inc.
- 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.
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