Methylphenidate Hydrochloride Tablets USP recall: Failed Dissolution
Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC…
Why was Methylphenidate Hydrochloride Tablets USP recalled?
Failed Dissolution Specifications: Low out of specification results for dissolution.
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?
Lot Number # 1156086M, Exp 08/18
- Product
- Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC…
- Recalling firm
- Teva Pharmaceuticals USA
- Quantity
- 58,292 bottles
- Distribution
- Nationwide in the USA and Puerto Rico
- Recall date
- November 1, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)