Medical Device Recall Database

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Medical Device Recalls - Food and Drug Administration

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

This database contains Medical Device Recalls classified since November 2002. Since January 2017, it may also include correction or removal actions initiated by a …

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 …

Medical Device Databases | FDA

https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/medical-device-databases

Apr 6, 2022

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

For additional information or technical assistance, you can contact Smith Medical’s Technical Assistance at 1- (800)-258-5361. Additional Resources: Medical …

International Medical Devices Database

https://medicaldevices.icij.org/

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers. Try Synchromed or St. Jude . …

Recalls, Corrections and Removals (Devices) | FDA

https://www.fda.gov/medical-devices/postmarket-requirements-devices/recalls-corrections-and-removals-devices

Recalls are classified into a numerical designation (I, II, or III) by the FDA to indicate the relative degree of health hazard presented by the product being recalled. Class I - a …

Medical Device Recalls - Food and Drug Administration

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

Medical Device Reports (MAUDE) CDRH Export Certificate Validation (CECV) CDRH FOIA Electronic Reading Room; CFR Title 21; CLIA; Device …

FDA Dashboards - Recalls - Food and Drug Administration

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

Important Note: Users can filter Recalls at either the Event or Product level. An event is a firm’s recall of one or more products. Filtering at the event level displays how many …

Emergent Recalls RSDL Kits Due to Leak Potential

https://www.fda.gov/medical-devices/medical-device-recalls/emergent-recalls-certain-rsdl-reactive-skin-decontamination-lotion-kits-due-leak-potential

Medical Device Recall Database entry How do I report a problem? Health care professionals and consumers may report adverse reactions or quality problems they …

Recall actions database | Therapeutic Goods …

https://www.tga.gov.au/recall-actions-database

30 June 2022 The Database is searchable for therapeutic good recall action notifications that include recalls, product defect corrections and hazard alerts (implanted medical …

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Medical Device Recalls - Food and Drug Administration

Medical Device Recalls | FDA

Medical Device Databases | FDA

Smiths Medical Recalls Certain CADD System …

International Medical Devices Database

Recalls, Corrections and Removals (Devices) | FDA

Medical Device Recalls - Food and Drug Administration

FDA Dashboards - Recalls - Food and Drug Administration

Emergent Recalls RSDL Kits Due to Leak Potential

Recall actions database | Therapeutic Goods …

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