Covidien Recalls Two Medical Devices

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Covidien, LLC (Medtronic) Recalls Palindrome and Mahurkar …

https://www.fda.gov/medical-devices/medical-device-recalls/covidien-llc-medtronic-recalls-palindrome-and-mahurkar-hemodialysis-catheters-due-catheter-hub

On June 8, 2022, Covidien, LLC (Medtronic) sent an Urgent Medical Recall Letter to affected customers informing them of the product issue and potential risks to health. Covidien, LLC (Medtronic) asked customers to take the following actions: 1. Immediately quarantine and discontinue use for specific lots of … See more

Class 2 Device Recall COVIDIEN Emprint Ablation Catheter with ...

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=197442

Class 2 Device Recall COVIDIEN Emprint Ablation Catheter with Thermosphere Technology. The product is labeled with the incorrect expiration date. …

Covidien Recalls Two Medical Devices - WSJ

https://www.wsj.com/articles/SB10001424052702303603904579495243062899118

Covidien PLC recalled two medical devices used to treat people with brain aneurysms, citing the potential for the devices to cause stroke or death. The company …

Class 2 Device Recall Covidien - accessdata.fda.gov

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=196699

Cause 2: Equipment maintenance: Action: Cardinal Health issued Urgent Medical Device Recall Letter (Event-2022-04944) and Acknowledgement Form on …

Class 2 Device Recall Covidien - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=188264

Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 …

Medtronic's Covidien faces another Class I recall of beleaguered ...

https://www.fiercebiotech.com/medtech/medtronic-s-covidien-faces-another-class-i-recall-beleaguered-puritan-bennett-ventilators

Medtronic's Covidien faces another Class I recall of beleaguered Puritan Bennett ventilators | Fierce Biotech Fierce Pharma Fierce Biotech Fierce Healthcare Fierce Life …

Class 2 Device Recall Covidien - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=185490

Covidien Llc 15 Hampshire St Mansfield MA 02048-1113: For Additional Information Contact: Catherine T. Wrenn 508-261-8000 Manufacturer Reason for Recall: …

Class 2 Device Recall Covidien Endo GIA Ultra Universal stapler

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=179451

COVIDIEN LLC 15 Hampshire St Mansfield MA 02048-1113: For Additional Information Contact: See Above 508-261-8000 Manufacturer Reason for Recall: Potential …

2022 Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls

11/01/22. Philips Respironics Recalls Certain Masks for BiPAP, CPAP Machines Due to Safety Issue ...

Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls

The FDA posts summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that …

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Covidien, LLC (Medtronic) Recalls Palindrome and Mahurkar …

Class 2 Device Recall COVIDIEN Emprint Ablation Catheter with ...

Covidien Recalls Two Medical Devices - WSJ

Class 2 Device Recall Covidien - accessdata.fda.gov

Class 2 Device Recall Covidien - Food and Drug Administration

Medtronic's Covidien faces another Class I recall of beleaguered ...

Class 2 Device Recall Covidien - Food and Drug Administration

Class 2 Device Recall Covidien Endo GIA Ultra Universal stapler

2022 Medical Device Recalls | FDA

Medical Device Recalls | FDA

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