Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC # 59746-339-90
Reported: August 6, 2014 Initiated: July 11, 2014 #D-1500-2014
Product Description
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC # 59746-339-90
Reason for Recall
Presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel.
Details
- Recalling Firm
- Jubilant Cadista Pharmaceuticals Inc.
- Units Affected
- 9,358 bottles
- Distribution
- Nationwide and Puerto Rico
- Location
- Salisbury, MD
Frequently Asked Questions
What product was recalled? ▼
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90-tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC # 59746-339-90. Recalled by Jubilant Cadista Pharmaceuticals Inc.. Units affected: 9,358 bottles.
Why was this product recalled? ▼
Presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 6, 2014. Severity: Moderate. Recall number: D-1500-2014.
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