| 
             
			
			 The company said on Wednesday its U.S. unit was recalling the 
			injections as they could potentially deliver an inaccurate dose. 
			 
			Auvi-Q is designed to treat anaphylaxis, a potentially fatal 
			allergic reaction, in patients who are at risk or who have a history 
			of such reactions. 
			 
			An incorrect dose could lead to significant health issues, Sanofi 
			said. 
			 
			The company has received 26 reports of suspected device malfunctions 
			in the United States and Canada as of Oct. 26. 
			 
			However, there has been no confirmation on the reports and no deaths 
			have been reported so far, Sanofi said. 
			 
			The company's U.S.-listed shares closed at $51.49 on the New York 
			Stock Exchange on Wednesday. 
			
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			(Reporting By Samantha Kareen Nair in Bengaluru; Editing by Anil 
			D'Silva and Kirti Pandey) 
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