Reported Sep 25, 2019 · Terminated
Fexofenadine HCL Tablets USP, 180 mg, 500's BRITE STOCK; Manufactured for: Aurohealth LLC., 2572 Brunswick Pike,…
Aurolife Pharma, LLC
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: Aurolife Pharma, LLC · 2400 US Highway 130 · Dayton, NJ · 08810-1519
Is this the product you have?
Fexofenadine HCL Tablets USP180 mg500's BRITE STOCK
- Manufactured forAurohealth LLC., 2572 Brunswick Pike, Lawrenceville, NJ 08648
- Manufactured byAurolife Pharma LLC, Dayton, NJ 08810
- Lot codes and dates
Lot #s:067180011A067180012AExp 04/2106718027B1Exp 09/21
- Amount recalled
- 6104 bottles
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
- Nationwide
Why it was recalled
Failed Impurities/Degradation Specifications
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.
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