Medical Recall

At Manningham Medical Centre, you can find all the data about Medical Recall. We have collected data about general practitioners, medical and surgical specialists, dental, pharmacy and more. Please see the links below for the information you need.

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 …

2023 Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/2023-medical-device-recalls

An official website of the United States government Here’s how you know U.S. Food and Drug Administration Search Menu Home Medical Devices Medical Device …

FDA eyes drugs with cancer-causing nitrosamines. What …

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

Dr. Yul Ejnes, a clinical professor of medicine at Alpert Medical School of Brown University, said people might panic and immediately stop their medication when …

U.S. FDA classifies recall of Philips' respiratory devices as most ...

https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-classifies-recall-philips-respiratory-devices-most-serious-2023-02-16/

2 days ago · The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of Dutch medical devices maker Philips' respiratory machines as most serious, …

GE HealthCare Recalls Nuclear Medicine Systems for …

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, …

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 …

Medical Device Recall Information - Philips Respironics …

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 …

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 …

Smiths Medical Issues Urgent Medical Device Correction …

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/smiths-medical-issues-urgent-medical-device-correction-letter-notifying-customers-potential-issues

Company Announcement MINNEAPOLIS, Dec. 12, 2022 /PRNewswire/ -- Smiths Medical issued an Urgent Medical Device Correction Letter to notify affected customers of two …

Need more information about Medical Recall?

At Manningham Medical Centre, we collected data on more than just Medical Recall. There is a lot of other useful information. Visit the related pages or our most popular pages. Also check out our Doctors page.