Reported Sep 25, 2019 · Terminated
Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 60000-409-53);…
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?
4 of 4 products
| # | Product as published |
|---|---|
| 1 | 15-count cartons (NDC 60000-409-53) |
| 2 | 30-count cartons (NDC 60000-409-30) |
| 3 | 45-count bonus cartons (NDC 60000-409-48) |
| 4 | 45-count cartons (NDC 60000-409-45); CAREone, Distributed by: Foodhold U.S.A., LLC, Landover, MD 20785. |
- Lot codes and dates
Lot #s: a) 067180025D1Exp 07/21b) 067180025B1Exp 07/21c) 067180025A1Exp 07/21d) 067180025C1Exp 07/21
- Amount recalled
- a) 9662 cartons; b) 7382 cartons; c) 5184 cartons; d) 9842 cartons
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.
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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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