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Harris Products Group recalls torch handles

Jul 31, 2014 ... Affected products What you should do Joint recall with Health Canada, the United States Consumer Product Safety Commission (US CPSC) and Harris Products Group Affected products Torch handles used for welding, cutting, brazing, soldering, and/or heating Product description This recall involves two models of torch handles that were manufactured from December 1, 2013

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Mar 30, 2012 ...: 2019-08-26 Type of communication: Recall Vinyl Protective Covers for Sunsetter Motorized Awnings recalled due to impact and fall hazard Consumers should immediately stop attempting to remove or install the recalled vinyl cover and contact the company to obtain a free safety clip repair kit. If you own a vinyl protective cover with bungee tie-downs, please

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Mar 30, 2012 ...-11-18 Type of communication: Recall Jean Coutu Duo Stem Recall (2013-11-18) Jean Coutu Duo Stem Recall (2013-11-18) Recalled Products A. Duo Stem anti accelerated aging serum B. Duo Stem Kit with anti accelerated aging serum + anti-wrinkle eye contour care C. Duo Stem anti-wrinkle eye contour care This product is considered a drug in Canada and was sold

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Mar 30, 2012 ... of communication: Recall Disposable gloves (2014-09-10) Disposable gloves (2014-09-10) Recalled products Disposable gloves Unlicensed disposable gloves were repackaged and added to first aid kits manufactured by F.A.S.T. A. Disposable gloves... Posted: 2014-09-10 Type of communication: Recall Infrared Coagulation System (IRC 2100) (2014-09-10) Infrared Coagulation System

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Mar 30, 2012 ...: 2012-02-29 Type of communication: Recall Hemocode Blood Collection Kit (February 29, 2012) Due to the placement of a lancet in the Hemocode Blood Collection Kit, the kit is an unlicensed Class II device. Users are being instructed to return the lancets to Gemoscan Canada or dispose of them in accordance to local regulations. 132863 1 Contact manufacturer Blood

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Mar 30, 2012 ... by telephone at 1-888-661-8201, by email or visit the firm's... Posted: 2016-12-05 Type of communication: Recall Devyser AZF Devyser AZF Sale of unlicensed class III medical device in Canada. Devyser AZF (8-A019) Kits were incorrectly labelled In Vitro Diagnostics (IVD) instead of Research Use Only (RUO). Devyser AZF... Posted: 2016-12-02 Type of communication: Recall

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