Camila 0.35 mg Tablets recall: Impurity Out of Spec
Camila 0.35 mg Tablets, 6 cards of 28 pills, Dist. By: Physicians Total Care, Tulsa, OK --- NDC 54868-4814-0, MFG By TEVA Pharmaceuticals USA…
Why was Camila 0.35 mg Tablets recalled?
Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Benzene Sulfonamide (NBBS) was detected during impurity testing
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Physicians Total Care Lots: 6Z4C Exp. 10/31/2013
- Product
- Camila 0.35 mg Tablets, 6 cards of 28 pills, Dist. By: Physicians Total Care, Tulsa, OK --- NDC 54868-4814-0, MFG By TEVA Pharmaceuticals USA…
- Recalling firm
- Physicians Total Care, Inc.
- Quantity
- 6 cards of 28 tablets
- Distribution
- MO
- Recall date
- June 5, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)