Recall RadarNicotine Transdermal System Patch, 14 mg, 14 patches per box, Aveva, Distributed by: RUGBY LABORATORIES, Indianapolis, IN 46268, www.majorpharmaceuticals.com, NDC 0536-5895-88.
Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of individual units.
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- AVEVA Drug Delivery Systems, Inc. — Miramar, FL
- Severity
- Class III — low
- Reported
- June 3, 2026
- Quantity
- 59,808 pouches (4,272 Individual Folding Carton (IFC))
- Recall number
- D-0550-2026
- Status
- Ongoing
- Source
- FDA
Where it went
Nationwide within the U.S
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