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Health Canada clarification: laser-based medical devices are not licensed in Canada to cure fungal nail infections

Dec 5, 2019 ... are not authorized to treat fungal nail infections (onychomycosis). Health Canada is clarifying that, while some laser-based medical devices are licensed in Canada to temporarily increase the clarity of the nail in patients with a fungal nail infection, none have been licensed to cure these infections. Canadians who have received laser treatments for their condition from

Vita-Mix Corporation recalls Ascent™ and Venturist™ Series 8-ounce and 20-ounce Blending Containers

Aug 9, 2018 .... Only containers marked with blade date codes March 2018 ("03-18") or earlier are included in this recall. If the blade base is marked on the bottom with a green or orange dot, the container has already been repaired. The blade date code is laser-etched onto the top of the blade in the blade base. Hazard identified The container can separate from the blade base

Huish Outdoors recalls Oceanic and Hollis Scuba Diving Regulators

Jun 26, 2018 ... a diver breathes. Only regulators with the following part numbers are included in the recall. The serial number is laser etched on the first stage body. Affected products are listed in the table below Product Name Part Number Description UPC Oceanic CDX First Stage 40-3770-07 ALPHA 10 + CDX, YOKE 020545096023 40-3771-07 ALPHA 10 + CDX, DIN 020545096030 40-3770 CDX


Sep 1, 2015 ... laser marking "RASH3N" along the body of the driver tip. Affected products A. DRIVERS AND DRIVER TIPS Lot or serial number 1184554 1184555 Model or catalog number RASH3N RASQ3N Companies Manufacturer BioMet 3I, also trading as Implant Innovations Inc. 4555 RIVERSIDE DRIVE Palm Beach Gardens 33410 Florida UNITED STATES Date modified: 2015-09-01

Elite XPL (Pulsed Light) Handpiece (2014-10-08)

Oct 22, 2014 ... Professionals, Hospitals Identification number: RA-41805 Reason Affected products Recalled Products Elite XPL (Pulsed Light) Handpiece Reason Cynosure has identified a potential situation where the user of the device could receive an electrical shock under certain conditions. If the laser system is turned on and the user adjusts, installs or removes the XPL pulsed light


... Identification number: RA-59016 Reason Affected products Affected products A. VISUALASE COOLED CATHETER LASER APPLICATOR Reason Manufacturer received reports of melting of the VCLAS catheters during procedures to ablate tissue. Manufacturer revised the recommended treatment parameters and revised and added warnings accordingly. Affected products A. VISUALASE COOLED

Boston Scientific Urgent Device Notification - Non-Sterile Devices Stolen and Risk of Infection - Notice to Hospitals

Mar 1, 2013 ..., endoscopic marking, anchoring jejunal feeding tubes or as a supplementary method for closure of GI tract luminal perforations. M00522612 ML000020C2 Pinnacle™ Pelvic Floor Repair Kit Pelvic Floor Repair Kit: Kits used for Pelvic Floor Repair of Pelvic Organ Prolapse M0068317050 ML00000034 Flexiva™ 365 High Power Single-Use Laser Fiber; Box 5 Fiber optic laser energy

“Konica Minolta” Colour Laser Printers

Dec 14, 2012 ... request alternate formats by contacting us. “Konica Minolta” Colour Laser Printers Report a Concern Starting date: April 16, 2012 Posting date: April 16, 2012 Type of communication: Consumer Product Recall Subcategory: Household Items, Miscellaneous Source of recall: Health Canada Audience: General Public (GP) Identification number: RA-500002810 Affected products

Mentor Gel Sizers (2014-05-27)

Jun 12, 2014 ..., Hospitals Identification number: RA-40001 Reason Affected products Recalled products Mentor Gel Sizers Reason A complaint was received for a volume discrepancy between the pad print (500cc) and laser engraved marking and all other product labeling (550cc) on a Mentor Gel Sizer. During the investigation, a second lot was identified as having a style discrepancy

Exeter Stem (Size 0)

... Affected products Reason Stryker has received customer inquiries stating that there were no laser etchings on the Exeter stem. Affected products Exeter Stem (Size 0) Lot or serial number G6106543 Model or catalog number 0580-1-440 Companies Manufacturer Howmedica Osteonics Corporation 325 Corporate Drive Mahwah 07430 UNITED STATES

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