Recall Radar5% Dextrose Injection, USP 12.5 g per 250 mL (50 mg per mL) 250 mL in a 250 mL freeflex bag, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Use NDC: 65219-458-05, Unit of Sal…
Lack of Assurance of Sterility
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 II — moderate
- Reported
- April 15, 2026
- Recall number
- D-0437-2026
- Status
- Ongoing
- Source
- FDA
Where it went
US Nationwide , Alaska, and Puerto Rico.
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