Advanced search

Find pages with...
Then narrow your results by...

About 25 search results

Important safety information on Duragesic (fentanyl transdermal system) - For Health Professionals - Janssen-Ortho Inc. - For Health Professionals

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2005/14319a-eng.php

Feb 8, 2013 ... temperature of 40°C (104°F) due to temperature-dependent increases in fentanyl release from the system and increased skin permeability. expose the DURAGESIC application site to direct external heat sources. All patients should be advised to avoid external heat sources such as heating pads, electric blankets, heated water beds, heat lamps, hot water bottles, saunas

Search results

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 ... SUPREMEGRAND PRIX,LUMINA CAR, and MONTE CARLO models GENERAL MOTORS issued a recall on the CUTLASS SUPREMEGRAND PRIX,LUMINA CAR, and MONTE CARLO models On certain vehicles, the spark plug wires may be causing the Malfunction Indicator Lamp (MIL) to be illuminated, as well as causing rough idle and poor performance. These conditions may be due to a dielectric... Posted

Search results

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=19000&plain_text=&s=

Mar 30, 2012 ... teethers until they have read the instructions on how to obtain a $10 credit certificate from Elfe Juvenile Products at the following web addresses: Playgro Toothy Teether Nuby™ Fun Pal... Posted: 2009-06-01 Type of communication: Recall Animated Ocean Lamp Consumers should immediately stop using the recalled product and contact Home Ideas. For more information

Search results

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=8000&plain_text=&s=

Mar 30, 2012 ..., the passenger airbag could deactivate, illuminating the airbag warning lamp and the passenger airbag... Posted: 2015-04-07 Type of communication: Recall KALMAR issued a recall on the OTTAWA model KALMAR issued a recall on the OTTAWA model On certain vehicles, movement of the primary battery ground cable could be restricted. This could cause the eyelet on the cable

Search results

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=25000&plain_text=&s=

Mar 30, 2012 ..., "lamps, reflective devices, and associated equipment." the owner's manual does not contain the proper headlamp aiming instructions. This does not meet the requirements of the... Posted: 2002-01-01 Type of communication: Recall VOLVO issued a recall on the TOW HITCH model VOLVO issued a recall on the TOW HITCH model A defect exits in the Brink Sverige AB

Search results

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=23000&plain_text=&s=

Mar 30, 2012 ... in the value sheet that are incorrect and may cause the patient results to shift such that treatment may not be initiated. 109621 1 20881M100 1E66-03 Clinical Chemistry Bilirubin Calibrator 2015-03-01 16:45:35 2015-03-01 16:45:35 Not Applicable... Posted: 2005-08-17 Type of communication: Recall Important Safety Information on Albumin Therapy in Critically-ill Patients

Search results

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=24000&plain_text=&s=

Mar 30, 2012 ... cross shaft and, if necessary, replace the throttle... Posted: 2004-01-01 Type of communication: Recall GENERAL MOTORS issued a recall on the ION model GENERAL MOTORS issued a recall on the ION model On certain vehicles, the turn signal/daytime running lamp (DRL) bulb on either front side can become inoperative because of inadequate contact between the bulb

Search results

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=20000&plain_text=&s=

Mar 30, 2012 ... of Desire product Lot # 0070263 and # 84881 obtained from a Canadian distributor contains Phentolamine as an undeclared ingredient which poses a Type I risk to health. Health food store 105023 1 Desire 0070263, 84881 Desire... Posted: 2008-06-02 Type of communication: Recall Archived - Safety information concerning Tensor Heat Therapy - For the Public Archived

Search results

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=21000&plain_text=&s=

Mar 30, 2012 ... Information - Subset of Implantable Cardiac Defibrillators and Cardiac Resynchronization Therapy Defibrillators For Health Professionals - Urgent Medical Device Information - Subset of Implantable Cardiac Defibrillators and Cardiac Resynchronization Therapy Defibrillators This is duplicated text of a letter from Boston Scientific. Contact the company for a copy of any

Search results

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=22000&plain_text=&s=

Mar 30, 2012 ...: Recall Lifepak 12 Defibrillator/Monitor and Lifepak 20 Defibrillator (March 24, 2006) Devices manufactured between October 2005 and February 2006 contain a therapy connector that may have connector sockets with short drill depths. 112147 1 More than 10 lot numbers, contact manufacturer Not applicable Lifepak 12 Defibrillator/Monitor 2015-03-01 16:47:25 2015-03-01

Report a problem or mistake on this page
Please select all that apply:

Thank you for your help!

You will not receive a reply. For enquiries, contact us.

Date modified: