Event Title Go back to Home Page
Event Summary  
Event Type Medicine - Misbranded/Mislabeled
Medicine - Pharmaceutical Recalls 
Date Time 2019-06-06 01:03:00 
Country US  City Torrance, CA 
Latitude 33.836  Longitude -118.341 
URL https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/enovachem-pharmaceuticals-issues-voluntary-nationwide-recall-dyural-40-and-dyural-80-convenience     
Description  
[fda.gov] CALIFORNIA - Enovachem Pharmaceuticals Issues Voluntary Nationwide Recall Of Dyural-40 And Dyural-80 Convenience Kits Containing Recalled Sodium Chloride Injection USP Point 9 Percent Due To Latex Hazard

"Torrance, CA, Asclemed USA Inc is voluntarily recalling 20 lots of Dyural-40 and 61 lots of Dyural-80, to the user level. The products include recalled Sodium Chloride, USP, 0.9% manufactured by Fresenius Kabi, which has been recalled due to product labeling incorrectly stating stoppers do not contain latex."

Read the full article:

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/enovachem-pharmaceuticals-issues-voluntary-nationwide-recall-dyural-40-and-dyural-80-convenience 

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