Fresenius Kabi USA, LLC recalls Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL Single Dose Bottle, Rx only,
Recalled December 16, 2020 · FDA recall D-0120-2021 · Fresenius Kabi USA
Hazard
Cross Contamination with other products: trace amounts of lidocaine · FDA Class I
Units
13,525 bottles
Sold at
USA Nationwide
Description
Cross Contamination with other products: trace amounts of lidocaine
Product
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
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →