FDAFDA · Food and drugs·Recall number D-1137-2017
Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534, NDC 68382-099-06, UPC 3 6838209906 8
Published September 20, 2017 · Recall initiated: August 18, 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
Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PAROXETINE
- Manufacturer
- Zydus Pharmaceuticals USA Inc
- Distributor
- Nationwide within United States
- UPC
- 0368382098108
- Lot
- Lot #: Z701133, Exp 03/19
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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