Cartia XT recall
Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufactured by: Watson Laboratories…
Why was Cartia XT recalled?
Presence of Foreign Substance; fine residue or dust identified as aluminum may be on exterior of the capsule shell
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 # 956000M, Exp. Aug 2016; UPC 3-6203760090-6
- Product
- Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufactured by: Watson Laboratories…
- Recalling firm
- Actavis Laboratories, FL, Inc.
- Quantity
- 2,628 bottles
- Distribution
- Nationwide
- Recall date
- April 22, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)