FDAFDA · Food and drugs·Recall number D-0120-2021
Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL Single Dose Bottle, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-671-05
Published December 16, 2020 · Recall initiated: November 17, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Cross Contamination with other products: trace amounts of lidocaine
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Fresenius Kabi USA, LLC
- Distributor
- USA Nationwide
- Lot
- Lot #: 6123925
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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