Aripiprazole Tablets recall: CGMP Deviations
Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, By; Hetero Hetero…
Why was Aripiprazole Tablets recalled?
CGMP Deviations: lot made with active pharmaceutical ingredient that did not meet all its intended specifications.
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 #: ARI17089, ARI17090, Exp. 5/2019
- Product
- Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, By; Hetero Hetero…
- Recalling firm
- Hetero Labs, Ltd. - Unit III
- Quantity
- 3000 bottles
- Distribution
- NJ Only
- Recall date
- February 14, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)