Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram- 603 110, Tamilnadu, India, NDC 64380-933-08
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot#: 7901903A, exp. date 04/2024
- 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:
- Strides Pharma Inc.
- Reason for Recall:
- Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram- 603 110, Tamilnadu, India, NDC 64380-933-08
Product Codes/Lot Numbers:
Lot#: 7901903A, exp. date 04/2024
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-0895-2023
Related Recalls
Failed Dissolution Specifications.
Presence of foreign substance: Presence of Benzene.
Presence of foreign substance: Presence of Benzene.