Dräger’s Breathing System Filter Recall Gets Class I Label from FDA After Ventilation Obstruction
Dräeger Medical, Inc. expanded on its voluntary recall of Lot LT2103 of Draeger SafeStar 55 Breathing System Filters.
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Search Results for: ventilator
GE Healthcare’s Recall of Ventilator Batteries Gets Class I Label from FDA Over Device Shutdown Risk
Due to their ability to cause the premature shutdown of GE Healthcare’s Carescape R860 ICU ventilators, the U.S. FDA has deemed GE Healthcare’s recall of more than 100,000 batteries as a Class 1 event—the most severe kind.
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Baxter Issues Urgent Medical Device Correction for Home Care System
Baxter has issued an Urgent Medical Device Correction for the home care Volara System to reinforce important safety information.
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FDA Gets Over 21,000 Medical Device Reports, Including 124 Deaths, Linked to Philips Foam Breakdown
The FDA updated a safety communication regarding medical device reports associated with the breakdown of materials used in Philips devices.
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US Med-Equip Expands to Offer On-Demand Medical Equipment for Silicon Valley
Medical equipment provider US Med-Equip is expanding to provide on-demand rentals and services from its new branch in San Jose, California.
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