Reported Jul 15, 2015 · Terminated
Losartan potassium tablets USP, 25 mg, 90- count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON…
Apotex Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Apotex Inc. · 150 Signet Drive · Toronto, N/A · N/A
Is this the product you have?
Losartan potassium tablets USP25 mg90- count bottleRx onlyManufactured for Apotex Inc 150 Signet DriveON M9L1T9 by Apotex Research Private LimitedPlot 1 & 2Bommasandra Industrial Area4th Phase Jigani Link RoadBangaloreKarnataka560099India NDC 60505-3160-9
- Lot codes and dates
Lot #: KP4726Exp date 9/2015
- Amount recalled
- 45,708 bottles
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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