Medical Recal

Medical Device Recalls | FDA

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

If you wish to find information on a recall, or a correction or removal action that has not yet been classified, you can search the Medical Device Recalls Database. Please note that the FDA...

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 with Magnets That May Affect Certain Medical Devices. 10/18/22. Jiangsu Well Biotech …

Medical Device Recall Information - Philips Respironics Sleep and ...

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update

The following products listed are affected by the recall notification / field safety notice: CPAP and BiLevel PAP Devices All Affected Devices Manufactured Before 26 April 2021, All Device Serial Numbers Continuous …

Covidien, LLC (Medtronic) Recalls Palindrome and …

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

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm

GE HealthCare Recalls Nuclear Medicine 600/800 Series …

https://www.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients

GE HealthCare Recalls Nuclear Medicine 600/800 Series Systems for Risk of Detector Fall That May Injure Patients The FDA has identified this as a Class I recall, the most …

Philips Respironics CPAP, BiPAP, and Ventilator Recall: FAQs

https://www.fda.gov/medical-devices/safety-communications/faqs-philips-respironics-ventilator-bipap-machine-and-cpap-machine-recalls

The FDA classified the June 2021 Philips recall of certain ventilators, BIPAP machines, and CPAP machines as a Class I recall, the most serious type of recall. Class I …

Recalls.gov

https://www.recalls.gov/medicine.html

The Food and Drug Administration (FDA)has jurisdiction over recalls involving the following: drugs vaccines medical devices other biologics blood and plasma products veterinary products FDA …

Smiths Medical Recalls Certain CADD System …

https://www.fda.gov/medical-devices/medical-device-recalls/smiths-medical-recalls-certain-cadd-system-administration-sets-and-cassette-reservoirs-issues

They deliver the medication into a patient’s vein or through other cleared routes of administration. Reason for Recall Smiths Medical is recalling certain CADD Administration …

FDA eyes drugs with cancer-causing nitrosamines. What …

https://www.usatoday.com/story/news/health/2023/02/16/fda-medication-drug-nitrosamines-evaluation/11219183002/

For people managing high blood pressure, recalls of the carcinogen-tainted drug quinapril might sound familiar. Since 2018, more than 12 million bottles of blood pressure …