Cataflam (diclofenac potassium) tablets, 50 mg, 100-count bottles, Rx only, Manufactured by: Patheon Inc., Whitby Operations, Ontario, Canada L1N 5Z5; Distributed by: Novartis Pharmaceuticals Corp., East Hanover, New Jersey 07936; NDC 0078-0436-05, UPC 3 0078-0436-05 2.
Reported: August 13, 2014 Initiated: July 30, 2014 #D-1516-2014
Product Description
Cataflam (diclofenac potassium) tablets, 50 mg, 100-count bottles, Rx only, Manufactured by: Patheon Inc., Whitby Operations, Ontario, Canada L1N 5Z5; Distributed by: Novartis Pharmaceuticals Corp., East Hanover, New Jersey 07936; NDC 0078-0436-05, UPC 3 0078-0436-05 2.
Reason for Recall
Failed Tablet/Capsule Specifications: Ink identification had rubbed off tablets in transit making them illegible to pharmacists and consumers.
Details
- Recalling Firm
- Novartis Pharmaceuticals Corp.
- Units Affected
- 50 bottles
- Distribution
- Nationwide
- Location
- Suffern, NY
Frequently Asked Questions
What product was recalled? ▼
Cataflam (diclofenac potassium) tablets, 50 mg, 100-count bottles, Rx only, Manufactured by: Patheon Inc., Whitby Operations, Ontario, Canada L1N 5Z5; Distributed by: Novartis Pharmaceuticals Corp., East Hanover, New Jersey 07936; NDC 0078-0436-05, UPC 3 0078-0436-05 2.. Recalled by Novartis Pharmaceuticals Corp.. Units affected: 50 bottles.
Why was this product recalled? ▼
Failed Tablet/Capsule Specifications: Ink identification had rubbed off tablets in transit making them illegible to pharmacists and consumers.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 13, 2014. Severity: Low. Recall number: D-1516-2014.
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