Metoprolol Succinate Extended-Release Tablets, USP, 25 mg Tablets, Packaged in A) 100 Count Bottles (NDC: 64679-0734-02), B) 500 Count Bottles (NDC: 64679-0734-03), C) 8000 Count Pouches, For Repacking Only (NDC: 64679-734-08) and D) 12 x 30 Tablet Dispenser Pack Cartons (NDC: 64679-0734-09), Rx Only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA.
Class I - DangerousWhat Should You Do?
- Check if you have this product: A) Lot #: LN11050, Expiry: 4/30/2015; Lot #: LN11053, Expiry: 4/30/2015; Lot #: LN11169, Expiry: 5/31/2015; Lot #: LN11312, Expiry: 6/30/2015; Lot #: LN11313, Expiry: 6/30/2015; Lot #: LN11318, Expiry: 6/30/2015. B) Lot #: LN11030, Expiry: 4/30/2015; Lot #: LN11031, Expiry: 4/30/2015; Lot #: LN11032, Expiry: 4/30/2015; Lot #: LN11038, Expiry: 4/30/2015; Lot #: LN11042, Expiry; 4/30/2015; Lot #: LN11047, Expiry: 4/30/2015; Lot #: LN11173, Expiry: 5/31/2015; Lot #: LN11289, Expiry: 6/30/2015; Lot #: LN11293, Expiry: 6/30/2015. C) Lot #: LN11185, Expiry: 5/31/2015; Lot #: LN11190, Expiry: 5/31/2015. D) Lot #: LN11180, Expiry: 5/31/2015.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Wockhardt Usa Inc.
- Reason for Recall:
- CGMP Deviations: Firm did not adequately investigate customer complaints.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Metoprolol Succinate Extended-Release Tablets, USP, 25 mg Tablets, Packaged in A) 100 Count Bottles (NDC: 64679-0734-02), B) 500 Count Bottles (NDC: 64679-0734-03), C) 8000 Count Pouches, For Repacking Only (NDC: 64679-734-08) and D) 12 x 30 Tablet Dispenser Pack Cartons (NDC: 64679-0734-09), Rx Only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA.
Product Codes/Lot Numbers:
A) Lot #: LN11050, Expiry: 4/30/2015; Lot #: LN11053, Expiry: 4/30/2015; Lot #: LN11169, Expiry: 5/31/2015; Lot #: LN11312, Expiry: 6/30/2015; Lot #: LN11313, Expiry: 6/30/2015; Lot #: LN11318, Expiry: 6/30/2015. B) Lot #: LN11030, Expiry: 4/30/2015; Lot #: LN11031, Expiry: 4/30/2015; Lot #: LN11032, Expiry: 4/30/2015; Lot #: LN11038, Expiry: 4/30/2015; Lot #: LN11042, Expiry; 4/30/2015; Lot #: LN11047, Expiry: 4/30/2015; Lot #: LN11173, Expiry: 5/31/2015; Lot #: LN11289, Expiry: 6/30/2015; Lot #: LN11293, Expiry: 6/30/2015. C) Lot #: LN11185, Expiry: 5/31/2015; Lot #: LN11190, Expiry: 5/31/2015. D) Lot #: LN11180, Expiry: 5/31/2015.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-1272-2015
Related Recalls
Failed Impurities/Degradation Specifications: 5mg strength being recalled for out of specification results for related compound.
CGMP Deviations: An FDA inspection identified inadequate investigations of past market complaints.
CGMP Deviations: An FDA inspection identified inadequate investigations of past market complaints.