Fresenius Kabi Issues Limited Ivenix LVP Recall
Fresenius Kabi recalled a specific lot of Ivenix LVP Primary Administration Sets due to a defect that could cause uncontrolled flow.
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Baxter Recalls Volara System Parts For Disconnection Issues
Baxter is recalling certain Volara System components due to a disconnection issue that may lead to insufficient ventilation.
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Defibtech Recalls Chest Compression Devices for Malfunction
Defibtech is recalling its RMU-2000 ARM XR Chest Compression Devices due to a motor issue that may cause the device to stop compressions, leading to potential patient injury or death.
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Tandem Diabetes Care Updates on Insulin Pump Battery Recall
Tandem Diabetes Care, Inc. provided an update on the t:connect app due to an issue causing rapid depletion of the tX2 insulin pump battery.
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Philips Files Lawsuit Against PSN Labs Over Foam Recall Damage
Philips has filed a lawsuit against PSN Labs, claiming incorrect analysis of foam material used in recalled ventilation devices.
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