Recall RadarEpinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-696-02 (vial), NDC 63323-696-25 (carton)
Failed Impurities/Degradations Specifications
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
- Fresenius Kabi USA, LLC — Lake Zurich, IL
- Severity
- Class III — low
- Reported
- June 17, 2026
- Quantity
- 898,050 vials
- Recall number
- D-0581-2026
- Status
- Ongoing
- Source
- FDA
Where it went
US Nationwide.
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