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.
Read MoreThe 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.
Read MoreSedgwick brand protection releases a year-in-review analysis of 2024 recall data, including the top five failures for medical devices.
Read MoreAbiomed has updated the use instructions for its Impella RP pumps due to a risk of device interaction that could damage the optical sensor or temporarily stop the pump.
Read MoreFeb 9, 2025 | Government Regulations | 0 |
IPEM backs the House of Lords Science and Technology Committee in calling for immigration reforms to support medical physics and clinical engineering.
Read MoreBaxter is replacing faulty battery chargers in the Life2000 Ventilator system after identifying a defect that triggers alarms and renders the device inoperable.
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