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Stampede Presentation Products (Canada) Inc. recalls Mustang Electronic Screen

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2015/53914r-eng.php

Jun 25, 2015 ... number: RA-53914 Affected products What you should do Affected products Mustang Electronic Screen Product description This recall involves Mustang electronic projection screens. The following model numbers are included in this recall: SC-E84D43, SC-E100D43, SC-E120D43, SC-E92D169, SC-E106D169, SC-E120D169 and SC-E135D169. Hazard identified The affected products

Toro Power Sweep Electric Blower

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2009/12687r-eng.php

Feb 15, 2013 ... and serial numbers can be found on a decal on the blower. The recalled blowers have the words "Toro Power Sweep" written on another decal on the product, and a black impeller fan, which can be seen through the air inlet screen on the bottom of the unit. The recalled electric blowers were manufactured between 2000 and 2002. For more information pertaining

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

Mar 30, 2012 ... Class I DNA Typing Tray - B*45... Posted: 2019-04-09 Type of communication: Recall Quidel Triage TOX Drug Screen Control 1 (2019-04-09) Quidel Triage TOX Drug Screen Control 1 (2019-04-09) Affected Products Quidel Triage TOX Drug Screen Control 1 Software programming error in displaying correct results. Quidel Triage TOX Drug Screen Control 1... Posted: 2019-04

Important Safety information on certain St. Jude Medical implantable cardiac defibrillators - For Health Professional

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2005/14362a-eng.php

Feb 8, 2013 ... tachycardia detection or therapy. This will be noted by a warning message on the programmer screen upon device interrogation. Low Probability of Occurrence Approximately 36,000 of the devices listed above have been implanted worldwide with approximately 26,000 of these devices still remaining in service. About 8,000 of these are in service in markets outside

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=6000&plain_text=&s=

Mar 30, 2012 ...: 6001-7000 of 30516 Previous Next DRUGCHECK DRUG SCREEN CUP (2016-03-30) DRUGCHECK DRUG SCREEN CUP (2016-03-30) Affected products A. DRUGCHECK DRUG SCREEN CUP Affected lots of EDIs drugs of abuse tests have shown reduced reactivity for up to three (3) of the nineteen (19) benzodiazepine compounds for which specificity information is provided in the product

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=4000&plain_text=&s=

Mar 30, 2012 ... Inspection Agency (CFIA) is conducting a food safety investigation, which may lead to the recall of other products. If other high-risk products are recalled, the CFIA will notify the public through updated Food Recall Warnings.The... Posted: 2017-03-11 Type of communication: Recall Rapidec Carba NP Rapidec Carba NP Confirmation of a screen printing error mentionned

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=10000&plain_text=&s=

Mar 30, 2012 ...Search interface for Health Canada website

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=14000&plain_text=&s=

Mar 30, 2012 ...Search interface for Health Canada website

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=7000&plain_text=&s=

Mar 30, 2012 ... PLATE HOLDER-LONG... Posted: 2015-10-06 Type of communication: Recall Plum 360 Infusion System with MedNet (2015-10-06) Plum 360 Infusion System with MedNet (2015-10-06) Affected Products When the user selects "yes" at the "new patient?" screen, and the program was not changed prior to powering off the infuser, the distal occlusion pressure setting is assigned

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=18000&plain_text=&s=

Mar 30, 2012 ... of communication: Recall KidLAX (March 31, 2010) No market authorization / Unacceptable risk to health identified during a market survey for children's products for the Compliance Monitoring Project. Wholesalers and Retailers 106423 1 KidLAX 16533, 17516, 19555, 20177, 23053, 24441 KidLAX 2015-03-01 16:42:41 2015-03-01 16:42:41 No market... Posted: 2010-03-31 Type

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