US Drug Recall Register
Class I · High risk Terminated Initiated Nov 17, 2020 (6 years ago)

Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Cross Contamination with other products: trace amounts of lidocaine

What was recalled

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

Recalling firm
Fresenius Kabi USA, LLC
NDC code
63323-671-05
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0120-2021

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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