Reported Oct 21, 2015 · Terminated
Equaline Original Prescription Strength, loratadine orally disintegrating tablets, USP, 10 mg, packaged in a) 10-count…
Ohm Laboratories, Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.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: Ohm Laboratories, Inc. · 1385 Livingston Ave · North Brunswick, NJ · 08902-1829
Is this the product you have?
Equaline Original Prescription Strengthloratadine orally disintegrating tabletsUSP10 mgpackaged in a) 10-count tablets per boxNDC 41163-528-69UPC 0 4116347138 2and b) 30-count tablets per boxNDC 41163-528-31UPC 0 4116346654 8
- Distributed bySupervalu Inc. Eden Prarie, MN 55344 USA
- Lot codes and dates
- Batch Numbers
a) 2617892Exp 5/31/20162625092Exp 6/30/201625444862544488Exp 7/31/20162600127Exp 2/29/20162644265Exp 9/30/2016 b) 25444862544488Exp 7/31/20162600127Exp 2/29/20162644265Exp 9/30/2016
- Batch Numbers
- Amount recalled
- 43,344 boxes
This recall covers 21 products
The agency filed one notice per product. You are reading one of them; the other 20 are below.
8 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Superpotent Drug: Out Of Specification (OOS) result for Assay.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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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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