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device recalls

FDA Deems Recall of Stolen Medtronic Laryngoscopes as Class I

FDA Deems Recall of Stolen Medtronic Laryngoscopes as Class I

Medical Devices and Diagnostics Industry

product recalls

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Thousands got Exactech knee or hip replacements. Then, patients say, the parts began to fail

Thousands got Exactech knee or hip replacements. Then, patients say, the parts began to fail

Medical Marketing and Media

joint replacements

product recalls

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Philips Scandal Is a Blight on Medtech's Reputation

Philips Scandal Is a Blight on Medtech's Reputation

Medical Devices and Diagnostics Industry

product recalls

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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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