FDA Issues Early Alert on Baxter Spectrum Infusion Pump Recall
The FDA has issued an early alert regarding Baxter’s recall of certain Spectrum infusion pumps due to missing motor mounting screws, which may have occurred during servicing.
The FDA has issued an early alert regarding Baxter’s recall of certain Spectrum infusion pumps due to missing motor mounting screws, which may have occurred during servicing.
Baxter announced an urgent issue with its Spectrum V8 and Spectrum IQ infusion pumps related to recent software updates.
Baxter has issued an Urgent Medical Device Correction for the home care Volara System to reinforce important safety information.
The FDA has issued an early alert regarding Baxter’s recall of certain Spectrum infusion pumps due to missing motor mounting screws, which may have occurred during servicing.
According to sources close to the matter, Deerfield, Ill.-based medical technology company Baxter is in talks to purchase Chicago-based Hill-Rom, which manufactures hospital beds and patient monitoring equipment.
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