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
Reported: July 12, 2023 Initiated: June 26, 2023 #D-0895-2023
Product 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
Reason for Recall
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
Details
- Recalling Firm
- Strides Pharma Inc.
- Units Affected
- 2,700 HDPE Bottles
- Distribution
- Nationwide in the USA.
- Location
- East Brunswick, NJ
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Strides Pharma Inc.. Units affected: 2,700 HDPE Bottles.
Why was this product recalled? ▼
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 12, 2023. Severity: Moderate. Recall number: D-0895-2023.
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