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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


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

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)

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


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

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

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

Canadian Tire Corporation Limited recalls MasterCraft Work Platform

Jun 30, 2016 ... do Affected products MasterCraft Work Platform Product description This recall involves the MasterCraft Work Platform. The product is 51 centimetres (20 inches) tall with a 30 X 91(12x36") centimetres non-slip deck and a 113 kg (250 lb) weight capacity. The platform doubles as a sawhorse or seating bench. The batch number can be found laser engraved on one

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

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

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

Mar 1, 2013 ... infection, if they suspect or know that the below stolen non-sterile devices have been used. Only the specific UPNs and Batches identified in the table below are affected. If you have any of these identified devices in your current inventory or receive any future delivery of these batches of devices, please do not use the devices and contact John Zagala (Quality

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