Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA --- NDC 62037-0600-90
Reported: April 22, 2015 Initiated: March 26, 2015 #D-0488-2015
Product Description
Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA --- NDC 62037-0600-90
Reason for Recall
Presence of Foreign Substance; fine residue or dust identified as aluminum may be on exterior of the capsule shell
Details
- Recalling Firm
- Actavis Laboratories, FL, Inc.
- Units Affected
- 2,628 bottles
- Distribution
- Nationwide
- Location
- Davie, FL
Frequently Asked Questions
What product was recalled? ▼
Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA --- NDC 62037-0600-90. Recalled by Actavis Laboratories, FL, Inc.. Units affected: 2,628 bottles.
Why was this product recalled? ▼
Presence of Foreign Substance; fine residue or dust identified as aluminum may be on exterior of the capsule shell
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 22, 2015. Severity: Low. Recall number: D-0488-2015.
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