Regulatorische Updates
9. Sept. 2026•1 Min. Lesezeit
FDA Approves Sodium Chloride Injection (NDA018090)
The FDA has approved NDA018090 for Sodium Chloride 0.45% injectable, manufactured by ICU Medical Inc.
Regulatorische Updates
8. Sept. 2026•1 Min. Lesezeit
FDA Approves Sorbitol-Mannitol (NDA018316) for Urethral Irrigation
The FDA has approved the prescription drug Sorbitol-Mannitol (NDA018316), a urethral irrigation solution containing mannitol and sorbitol, manufactured by ICU Medical Inc.
Regulatorische Updates
28. Aug. 2026•1 Min. Lesezeit
ICU Medical Canada Recalls Certain IV Sets Due to Possible Discoloration
ICU Medical Canada is recalling IV sets with potential discoloration in the drip chamber; products remain usable per facility protocol.
Regulatorische Updates
28. Aug. 2026•1 Min. Lesezeit
ICU Medical Canada recalls IV sets due to possible drip chamber discoloration
ICU Medical Canada is recalling certain IV sets because discoloration may appear in the drip chamber, though they remain usable per protocol.
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