Medical Recalls 2012

Medical Device Recalls | FDA

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

Summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that they could cause serious health problems or death.

Medical Device Recalls - Food and Drug Administration

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

FDA Dashboards - Recalls - Food and Drug Administration

https://datadashboard.fda.gov/ora/cd/recalls.htm

Only recalls classified on or after 06/08/2012 are displayed on the dashboard. For detailed information about individual recalls, please see the Enforcement Reports and public releases and public notices. Show more/Show less. Important Note: Users can filter Recalls at either the Event or Product level. An event is a firm’s recall of one or ...

Recalls.gov

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

medical devices; other biologics blood and plasma products; veterinary products. FDA Recalls and Safety Alerts: ... This site is provided as a resource for federal recalls. …

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/textsearch.cfm

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/resCollection_2.cfm?ID=114595

Medical Device Recalls: Date Initiated by Firm: November 19, 2012: Create Date: December 14, 2012: Recall Status 1: Terminated 3: Recall Number: Z-0514-2013: Recall Event ID: 63710: Product: Patient Circuit used with the Life Pulse High Frequency Ventilator. The Patient Circuit is a required disposable component of the Life Pulse High …

Medical Device Recall Report - FDAnews

https://www.fdanews.com/ext/resources/files/03/03-31-14-Recalls.pdf

Medical device recall information was collected, reviewed, and analyzed for the period encompassing FY 2003 through FY 2012. Concerted efforts to improve the quality and safety of medical devices on the part of both CDRH and industry has resulted in greater numbers of recalls reported - and greater benefit for the public health. Some of the

It's Your Week: FDA recalls since 2012 - msn.com

https://www.msn.com/en-us/health/other/its-your-week-fda-recalls-since-2012/ar-AA17BAMe

It's Your Week: FDA recalls since 2012. In December, four lots of the blood pressure medication Quinapril were recalled by the manufacturer Lupin Pharmaceuticals Inc. due …

2023 Medical Device Recalls | FDA

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

2022 Medical Device Recalls. Device Name. Date. Smiths Medical Recalls Certain CADD System Administration Sets and Cassette Reservoirs for Issues Causing …

Medical device recalls for September 2012 - MassDevice

https://www.massdevice.com/medical-device-recalls-september-2012/

Class I recalls Recalling Manufacturer, Date Posted, Trade Name/Product, Reason for Recall Custom Medical Specialties; Inc. Sep-20-2012 Povidine-Iodine prep …