Baxter Healthcare Corporation recalls Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Inject
See all recalls from Baxter Healthcare Corporation →Recalled Product
Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in Galaxy 100 mL Single Dose Container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-9557-12.
Hazard / Issue
CGMP Deviations
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot # NC188654, Exp Date: 08/31/2027; Lot # NC188821, Exp Date: 09/30/2027; Lot # NC193658, NC193702, Exp Date: 01/31/2028.
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Dexmedetomidine Hydrochloride in 0.9% →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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