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For the Public - Possible Association of Remicade (infliximab) with hepatosplenic T-cell lymphoma in pediatric and young adult patients with Crohn's disease

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2006/14201a-eng.php

Mar 4, 2013 ..., pregnant or breast feeding women Source of recall: Health Canada Audience: General Public Identification number: RA-19000461 The Health Products and Food Branch (HPFB) posts on the Health Canada web site safety alerts, public health advisories, press releases and other notices as a service to health professionals, consumers, and other interested parties

Important Safety Information on PediCap Pediatric End-Tidal CO2 Detectors - Notice to Hospitals

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2009/14563a-eng.php

Mar 5, 2013 ... professionals and consumers reporting them. Reporting rates determined on the basis of spontaneously reported post-marketing adverse incidents are generally presumed to underestimate the risks associated with health product treatments. Any cases of serious specific adverse incident or other serious adverse incidents in patients using PediCap End-Tidal CO2 Detectors

For the Public - Recall of certain lots of SureStep Blood Glucose Meters

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2006/14203a-eng.php

Mar 5, 2013 ... request alternate formats by contacting us. For the Public - Recall of certain lots of SureStep Blood Glucose Meters Report a Concern Starting date: April 13, 2006 Posting date: June 22, 2006 Type of communication: Public Communication Subcategory: Medical Device Source of recall: Health Canada Audience: General Public Identification number: RA-19000471 Images

Duet TRS Loading Units (Used with Endo GIA Universal Staplers and Endo GIA Universal Ultra Staplers) - Urgent Medical Device Recall - Contraindication for Thoracic Use - Notice to Hospitals

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2012/14677a-eng.php

Apr 30, 2013 ... reporting them. Reporting rates determined on the basis of spontaneously reported post-market adverse incidents are generally presumed to underestimate the risks associated with health product treatments. Any cases of serious injury or other serious or unexpected adverse incidents for medical devices in patients using Duet TRS™ Single Use Loading Units should

Level 1 Normothermic I.V. Fluid Administration Sets equipped with F-50 Gas Vent Filter Assembly - Market Withdrawal - Notice to Hospitals

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2011/14645a-eng.php

Mar 21, 2013 ... purposes only. If you wish to use the form, you must use the alternate format below. Help on accessing alternative formats, such as Portable Document Format (PDF), Microsoft Word and PowerPoint (PPT) files, can be obtained in the alternate format help section. Notice to Hospitals Health Canada Endorsed Important Safety Information on Level 1 Normothermic I.V. Fluid

Recall Notice, Portex Uncuffed Pediatric-Sized Tracheal Tubes - For Health Professionals

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2009/14568a-eng.php

Mar 18, 2013 ... marketed health product-related adverse incidents depends on health care professionals and consumers reporting them. Reporting rates determined on the basis of spontaneously reported post-marketing adverse incidents are generally presumed to underestimate the risks associated with health product treatments. Any cases of adverse incidents in patients using Portex

Important Safety Information on Hospira Devices that have Defective AC Power Cords

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2009/14553a-eng.php

Mar 18, 2013 ... care professionals and consumers reporting them. Reporting rates determined on the basis of spontaneously reported post-marketing adverse incidents are generally presumed to underestimate the risks associated with health product treatments. Any cases of serious specific adverse incident or other serious adverse incidents in patients using Hospira devices

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Mar 30, 2012 ... without warning. The resultant loss of propulsion, in conjunction with traffic and... Posted: 2010-01-01 Type of communication: Recall GENERAL MOTORS issued a recall on multiple vehicle models GENERAL MOTORS issued a recall on multiple vehicle models On certain vehicles, the rear axle cross pin was improperly heat treated (during the manufacturing process

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=26000&plain_text=&s=

Mar 30, 2012 ... WHICH COULD RESULT IN A SHORT CIRCUIT ON THE STARTER TERMINAL AND A POSSIBLE ENGINE COMPARTMENT FIRE.CORRECTION:... Posted: 1998-01-01 Type of communication: Recall GENERAL MOTORS issued a recall on the SILHOUETTE and VENTURE models GENERAL MOTORS issued a recall on the SILHOUETTE and VENTURE models NOTE: VEHICLES EQUIPPED WITH BUCKET SEATS OR A SPLIT BENCH SEAT

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=0&plain_text=&s=

Mar 30, 2012 ... Healthcare Diagnostics has confirmed that a communication error could be generated on the system application software when using the ASTM interface protocol to connect with laboratory information system (LIS).... Posted: 2019-09-13 Type of communication: Recall RW Consumer Products Ltd. Gripe Water Product Recall (2019-09-13) RW Consumer Products Ltd. Gripe Water

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