Reported Jul 15, 2015 · Terminated
Losartan potassium tablets USP, 50 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 USP50 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 60505-3161-9
- Lot codes and dates
Lot #: KN1449Exp 06/2015
- Amount recalled
- 23,076 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.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Apotex Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.