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

http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67326r-eng.php

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

VISUALASE COOLED CATHETER LASER APPLICATOR (2016-05-27)

http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2016/59016r-eng.php

Jun 24, 2016 ... 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

Huish Outdoors recalls Oceanic and Hollis Scuba Diving Regulators

http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67060r-eng.php

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

Exeter Stem (Size 0)

http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/63158r-eng.php

May 2, 2017 ... 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 Date modified: 2017-05-02

DRIVERS AND DRIVER TIPS (2015-08-10)

http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2015/54862r-eng.php

Sep 1, 2015 ... Professionals, Hospitals Identification number: RA-54862 Reason Affected products Affected Products DRIVERS AND DRIVER TIPS  Reason The production documentation for the impacted items was inadvertently swapped during manufacturing. This caused the packaging labels to be created and applied incorrectly. Additionally, because of the swap, the RASQ3N received the RASH3N's

DRIVERS AND DRIVER TIPS (2015-08-10)

https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2015/54862r-eng.php

Sep 1, 2015 ... Professionals, Hospitals Identification number: RA-54862 Reason Affected products Affected Products DRIVERS AND DRIVER TIPS  Reason The production documentation for the impacted items was inadvertently swapped during manufacturing. This caused the packaging labels to be created and applied incorrectly. Additionally, because of the swap, the RASQ3N received the RASH3N's

Fox Factory, Inc. recalls Mountain Bike Shock Absorbers

http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2016/60774r-eng.php

Nov 1, 2016 ... connected to the blue compression and red rebound adjusters that have "X2" and "RVS" laser etched on them. Recalled shocks do not have a “250 psi max” label directly under the air fill boss on the outer sleeve of the shock. A full listing of all recalled shocks and bicycle models can be found on the company's website. Hazard identified The bicycle's rear shock

Hand-held Lasers or Laser Pointers May Cause Serious Vision Damage If Used Improperly

http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2011/13529a-eng.php

May 1, 2013 ... or in any other application unless operated by individuals who have been professionally trained in laser safety. Report health or safety concerns Health Canada is interested in receiving reports of incidents or injury reports related to consumer products and cosmetics that have been previously recalled (health and safety related complaints). Incidents or injuries

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https://healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=5&per_page=7900&plain_text=&s=

Mar 30, 2012 ...: 7901-7905 of 29152 Previous Next Elite XPL (Pulsed Light) Handpiece (2014-10-08) Elite XPL (Pulsed Light) Handpiece (2014-10-08) Recalled Products Elite XPL (Pulsed Light) Handpiece 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

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https://healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=5&per_page=26730&plain_text=&s=

Mar 30, 2012 ... OF VEHICLE CONTROL. CORRECTION: TIRES WILL BE REPLACED. Defect, Investigation,... Posted: 1990-01-01 Type of communication: Recall CHRYSLER issued a recall on the LASER and TALON models CHRYSLER issued a recall on the LASER and TALON models NON-STANDARD USE OF THE LATCH HANDLE COULD CAUSE SUN ROOF DISENGAGEMENT FROM THE ROOF DUE TO MALE HINGE DISENGAGEMENT FROM ITS

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