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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
Medtech
Medtronic
laryngoscopes
product recalls
device recalls
FDA
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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
Exactech
Medtech
joint replacements
product recalls
device 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
Philips
Medtech
Respironics
device recalls
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
Medtech
JNJ
Abiomed
Impella
product recalls
device 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
Medtech
Medtronic
FDA
device recalls
hemodialysis
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Philips' Latest Ventilator Recall
Philips' Latest Ventilator Recall
Medical Devices and Diagnostics Industry
Philips
ventilator
device recalls
Medtech
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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
JNJ
Abiomed
TAVR
Impella
device recalls
Medtech
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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
JNJ
Abiomed
Impella
TAVR
device recalls
Medtech
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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
Medtronic
Medtech
device recalls
ICDs
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
Medtech
JNJ
Ethicon
electrodes
device recalls
electrosurger
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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
Medtech
devices manufacturing
device recalls
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Philips can't catch a break
Philips can't catch a break
Medical Devices and Diagnostics Industry
Philips
device recalls
Medtech
Trilogy Evo
ventilators
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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
JNJ
Abiomed
devices
Medtech
Impella 5.5
product recalls
device 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
devices
Medtech
device recalls
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
Medtech
devices
high-risk devices
product recalls
device 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
Abbott Labs
device recalls
Medtech
diabetes
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
Medtech
Philips
CPAP
BiPAP
product recalls
device 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
devices
Medtech
device recalls
FDA
regulatory
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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
devices
Medtech
Philips
BiPAP machines
FDA
device recalls
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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
devices
Medtech
Philips
sleep apnea
device recalls
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