Device Recall
FDA•CRITICAL
Philips Respironics Trilogy Evo O2 Ventilator
Philips Respironics recalls Trilogy Evo O2 ventilators (SW 1.05.15.00) over delayed obstruction alarm.
4 productsPhilips Respironics recalls Trilogy Evo O2 ventilators (SW 1.05.15.00) over delayed obstruction alarm.
4 products
Merit Medical recalls CentrosFLO Hemodialysis Catheters over sheath introducer defect that may cause hemorrhage and other serious complications.
5 products
Baxter is issuing a correction for the Volara Respiratory Therapy system adapter module to prevent oxygen desaturation and lung injury.

Abiomed is recalling Generation 1 purge cassettes due to an increased risk of purge leaks.
2 products
Abiomed is recalling Automated Impella Controllers due to a potential delay in the "Purge System Blocked" alarm.
2 productsPhilips Respironics recalls Trilogy Evo ventilators over tidal volume discrepancy with non-pneumatic nebulizers.
4 products
Handy Solutions Neck & Shoulders Heating Pad (Model 25607) may overheat and cause burns if folded or placed under the body.

Erbe USA recalls Flexible Cryoprobes because probes may rupture or burst during use.
4 products
Insulet is recalling Omnipod 5 Pods due to a cannula defect that can cause insulin under-delivery and severe health risks.

Abiomed recalls Impella RP Flex with SmartAssist due to sensor drift risk.
3 products
Olympus is recalling the UHI-3 High Flow Insufflation Unit due to a software issue that may cause dangerous overpressure events.
3 products
Trividia recalls TRUE METRIX meter instructions over inadequate E-5 error guidance.
7 products