Catapres .2 recall: Failed Dissolution
Catapres .2 (clonidine hydrochloride, USP) 0.2mg, 100-count bottles, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT…
Why was Catapres .2 recalled?
Failed Dissolution Specifications: OOS resultsduring routine stability 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?
Lot: 757739, EXP 9/2020
- Product
- Catapres .2 (clonidine hydrochloride, USP) 0.2mg, 100-count bottles, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT…
- Recalling firm
- Boehringer Ingelheim Pharmaceuticals, Inc.
- Quantity
- 1,380 100-count bottles
- Distribution
- Distributed nationwide in the USA and Puerto Rico
- Recall date
- November 7, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)