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device recalls

J&J’s Abiomed updates labeling for certain Impella heart pumps in Class I safety event

J&J’s Abiomed updates labeling for certain Impella heart pumps in Class I safety event

Fierce Biotech

product recalls

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Medtronic’s dialysis device recall assigned to Class I by the FDA

Medtronic’s dialysis device recall assigned to Class I by the FDA

Medtech Dive

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Philips' Latest Ventilator Recall

Philips' Latest Ventilator Recall

Medical Devices and Diagnostics Industry

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J&J flags potential interference between heart pump and TAVR stents in recall

J&J flags potential interference between heart pump and TAVR stents in recall

Medtech Dive

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Abiomed’s Impella System Hit with Another Recall

Abiomed’s Impella System Hit with Another Recall

Medical Devices and Diagnostics Industry

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Medtronic recalls nearly 350,000 defibrillators for risk of reduced shock

Medtronic recalls nearly 350,000 defibrillators for risk of reduced shock

Medtech Dive

CRT-defibrillators

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J&J's Ethicon Faces Mega Electrode Recall

J&J's Ethicon Faces Mega Electrode Recall

Medical Devices and Diagnostics Industry

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Medical Device Recalls Linked to Unprecedented Level of Faulty Manufacturing

Medical Device Recalls Linked to Unprecedented Level of Faulty Manufacturing

Medical Devices and Diagnostics Industry

devices manufacturing

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Philips can't catch a break

Philips can't catch a break

Medical Devices and Diagnostics Industry

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Abiomed heart pump recall labeled Class I by FDA, no deaths reported

Abiomed heart pump recall labeled Class I by FDA, no deaths reported

Medtech Dive

product recalls

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Integra recalls all devices made at Boston facility in the past 5 years, pauses production

Integra recalls all devices made at Boston facility in the past 5 years, pauses production

Medtech Dive

Integra LifeSciences

postoperative fever

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Post-approval modification of high-risk devices linked to 30% jump in recall risk: study

Post-approval modification of high-risk devices linked to 30% jump in recall risk: study

Medtech Dive

high-risk devices

product recalls

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Abbott’s CGM Readers Face Class I Recall Over Lithium-ion Battery Issues

Abbott’s CGM Readers Face Class I Recall Over Lithium-ion Battery Issues

Medical Devices and Diagnostics Industry

FreeStyle Libre

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FDA warns some Philips respirators may not deliver the right treatment

FDA warns some Philips respirators may not deliver the right treatment

Stat

product recalls

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Expert: Studies linking recalled 510(k) devices to problematic predicate products are ‘warning shot’ for manufacturers

Expert: Studies linking recalled 510(k) devices to problematic predicate products are ‘warning shot’ for manufacturers

RAPS.org

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Philips’ latest BiPAP machine recall labeled Class I event by FDA

Philips’ latest BiPAP machine recall labeled Class I event by FDA

Medtech Dive

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Philips recalls 17M sleep apnea masks over magnets that could affect implanted devices

Philips recalls 17M sleep apnea masks over magnets that could affect implanted devices

Medtech Dive

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What is the impact of Philips' recall of sleep apnea devices?

What is the impact of Philips' recall of sleep apnea devices?

Reuters

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Medical device recalls hit two-year high in Q2, report finds

Medical device recalls hit two-year high in Q2, report finds

Medtech Dive

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BD’s recall of emergency vascular access devices labeled Class I event label by FDA

BD’s recall of emergency vascular access devices labeled Class I event label by FDA

Medtech Dive

Becton Dickinson

product recalls

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