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Percutaneous Radiofrequency Ablation Catheter and the Potential Risk of Atrioesophageal Fistula

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/66492a-eng.php

Aug 10, 2018 ... of the rare but serious risk of atrioesophageal fistula (AEF) associated with percutaneous radiofrequency (RF) ablation catheters that are used for the treatment of atrial fibrillation (AF). AEF usually occurs within 1 to 6 weeks following an AF ablation procedure using these catheters. While rare, AEF is associated with high morbidity and mortality. Early symptoms

Easton Axis Arrows

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2013/34241r-eng.php

Jun 19, 2013 ... recall with Health Canada, the United States Consumer Product Safety Commission (US CPSC) and Easton Technical Products. Affected products Easton Axis Arrows Product description This recall involves Easton Axis arrows in the following four different sizes and batch numbers: Easton Axis Arrows affected by this recall Size Batch Number 300 13169686 340 13170143 400

282 MEP (meprobamate-containing medicine) - Market Withdrawal, Effective October 28, 2013 - For Health Professionals

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2013/35311a-eng.php

Aug 29, 2013 ... MEP® is indicated for the relief of pain of various origins, accompanied by muscle spasm and anxiety. Each 282 MEP® tablet contains as medicinal ingredients acetylsalicylic acid (350 mg), codeine phosphate (15 mg), meprobamate (200 mg), and caffeine (15 mg, equivalent to 30 mg caffeine citrate). Following the review of safety and efficacy information for 282

Update on use of "Simply Thick" for infants

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2012/15074a-eng.php

Jan 29, 2013 ... enquiries Health Canada is advising parents and caregivers to consult their health professional before using Simply Thick to feed infants. This updates previous advice that focused on the use of this product for premature infants. Simply Thick is a xanthan gum-based product marketed for the management of swallowing disorders. It can be added to thicken liquids

282 MEP (meprobamate-containing medicine) - Market Withdrawal, Effective October 28, 2013 - For the Public

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2013/35313a-eng.php

Aug 29, 2013 ... phosphate, and caffeine. A safety review conducted by Health Canada has concluded that there is a risk of overdose, abuse and misuse with medicines containing meprobamate, such as 282 MEP®. A review of benefits and risks of 282 MEP®, mostly focused on its meprobamate content, found that there was not enough evidence of benefit to continue using this drug. 282 MEP

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Mar 30, 2012 ... Bloodlines model number 114510. 138179 1 1000023504, 1000024496, 1000024497, 1000027119, 1000027120, 1000038242 114510 Cartridge with Hemoscan (2013-02-15)... Posted: 2013-02-15 Type of communication: Recall DASH Patient Monitors and Port 2 (February 15, 2013) GE Healthcare became aware of the following issues affecting Dash 3000/4000/5000 patient monitors and Dash

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