Health Canada Medical Device Recall Database

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Recalls - Canada.ca

(5 days ago) The Recalls and Safety Alerts Database provides easy access to a comprehensive list of recalls, advisories, and safety alerts. This database includes recalls … See more

https://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/recalls.html

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Search the Canada Vigilance Adverse Reaction Online Database

(9 days ago) WebFrom Year (s) To Year (s) 3. Suspect Health Product Search Criteria. Help with Suspect Health Product Search Section. Section 3 is mandatory if Section 4 (below) …

https://cvp-pcv.hc-sc.gc.ca/arq-rei/index-eng.jsp

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Adverse reactions, medical device incidents and health product …

(1 days ago) Webidentifying and flagging duplicate reports in the Canada Vigilance database; cleaning the data so it can be analyzed; using automated data entry to reduce human error; 32 …

https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/adverse-reactions-incidents-recalls-2019-summary.html

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Medical Device Respirator recalls - Recalls and safety alerts

(4 days ago) WebThis table is a summary of the products Health Canada has asked companies to voluntarily recall/relabel, along with any associated distributors or importers who have confirmed to …

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73137a-eng.php?from=groupmessage&isappinstalled=0

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Find recalls, advisories and safety alerts - Canada.ca

(6 days ago) WebLatest recalls and safety alerts. Easy Eats Pandemanila brand Kalihim (Philippine Bread Rolls) recalled due to undeclared egg. Recall Food recall warning 2024-05-18. …

https://recalls-rappels.canada.ca/en

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Advanced search – Recalls, advisories and safety alerts – Canada.ca

(2 days ago) WebIntegra Cranial Kit. RecallHealth product recall 2024-05-08. Vyaire Medical Twin Tube Probenschlauch. RecallHealth product recall 2024-05-08. Unauthorized sexual …

https://recalls-rappels.canada.ca/en/search/site?f%5B0%5D=category%3A180

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Medical Device Incidents - Drug and Health Product Register

(9 days ago) WebReport a medical device problem (for health care professionals) Prescription Drug List; About . Questions and Answers - Prescription Drug List; Feedback; Search Medical …

https://hpr-rps.hres.ca/mdi_landing.php

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Continuous Positive Airway Pressure (CPAP), Bi-Level Positive …

(6 days ago) WebMedical Device Recall Subcategory: Medical Device Hazard classification: Type I Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare …

https://recalls-rappels.canada.ca/en/alert-recall/continuous-positive-airway-pressure-cpap-bi-level-positive-airway-pressure-bipap-and-0

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Medical Devices Drug and Health Products Portal

(2 days ago) WebReport a medical Device Problem (For Health Care Professionals) The incident reporting provisions in the Medical Device Regulations are intended to improve monitoring and …

https://dhpp.hpfb-dgpsa.ca/medical-devices

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Medical Devices Active Licence Listing (MDALL) - Canada.ca

(8 days ago) WebDevice Identifier is a unique series of letters or numbers or a combination of both, assigned by the manufacturer to identify the device. The catalogue number of the device is often …

https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/licences/medical-devices-active-licence-listing.html

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Health Canada recalls multiple medical devices including one that …

(3 days ago) WebHealth Canada says specific units are being recalled due to a possible sterility breach. View image in full screen A list of the various serial and model numbers of …

https://globalnews.ca/news/10399989/health-care-products-recalled-canada/

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Safety information International Medical Device Regulators Forum

(Just Now) WebDatabase of Adverse Event Notifications (DAEN) Medical devices safety Medical Devices Safety Update Alertas: Recall actions: Technovigilance: Canada: Advisories, …

https://www.imdrf.org/safety-information

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International Medical Devices Database

(2 days ago) WebInternational Medical Devices Database. By the International Consortium of Investigative Journalists. Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices …

https://medicaldevices.icij.org/

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Health Canada Guidance on Medical Device Recalls: Reporting and

(8 days ago) WebHealth Canada, a country’s regulating authority in healthcare products, has published a guidance document dedicated to recalls. The document provides an …

https://www.regdesk.co/health-canada-guidance-on-medical-device-recalls-reporting-and-terminology/

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Health Canada Guidance on Medical Device Recalls: Overview

(1 days ago) WebScope and Applicability. This guidance is addressed to various stakeholders within the medical device sector, including manufacturers, importers, and distributors. It …

https://www.regdesk.co/health-canada-guidance-on-medical-device-recalls-overview/

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Health Canada Guidance on Recalls: Basics RegDesk

(4 days ago) WebJul 22, 2021. Health Canada, the country’s regulating authority in the sphere of medical devices, has published a guidance document dedicated to medical device recalls. The …

https://www.regdesk.co/health-canada-guidance-on-recalls-basics/

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Medical Device Recalls - Food and Drug Administration

(4 days ago) WebMedical Device Recalls. This database contains Medical Device Recalls classified since November 2002. Since January 2017, it may also include correction or …

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

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Canada Gazette, Part 1, Volume 157, Number 15: Regulations …

(1 days ago) WebUsing a 2017 paper footnote 3 on medical device recalls in Canada from 2005 to 2015, it was found that there were 7 226 medical device recalls over a 10-year …

https://canadagazette.gc.ca/rp-pr/p1/2023/2023-04-15/html/reg1-eng.html

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Philips Respironics, Inc. Recalls Trilogy Evo Continuous Ventilators

(5 days ago) WebThis could cause serious adverse health consequences, including hypoventilation and death. As of May 13, 2024, Medical Device Recall Database …

https://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-inc-recalls-trilogy-evo-continuous-ventilators-due-software-related-possible

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Class 2 Device Recall HeartSine - accessdata.fda.gov

(4 days ago) Web1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the …

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=206255

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