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da Vinci S/Si and da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors (2018-08-06)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67400r-eng.php

Aug 17, 2018 ... the proximal edge of the extension tube, potentially attributed to mishandling and misuse as defined by the Instrument and Accessories User Manual. These cracks may fracture the plastic surrounding the instrument shaft, and may cause fragments of the extension tube to fall, including potentially into the patient. Affected products A. da Vinci S/Si EndoWrist 8mm

Y Tubing Optistar/Coiled Extension Tubing, Optistar Mr. Injection System and Optistar Le Contrast Delivery System (February 14, 2012)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2012/11311r-eng.php

Mar 1, 2015 ... request alternate formats by contacting us. Y Tubing Optistar/Coiled Extension Tubing, Optistar Mr. Injection System and Optistar Le Contrast Delivery System (February 14, 2012) Report a Concern Starting date: February 14, 2012 Posting date: March 19, 2012 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II

8mm Monopolar Curved Scissors (2018-10-22)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/69940r-eng.php

May 17, 2019 ... number: RA-69940 Last updated: 2019-05-17 Reason Affected products Affected Products 8mm Monopolar Curved Scissors Reason Specific versions of the Monopolar Curved Scissor (MCS) instruments can become distorted at the tube extension during sterilization, resulting in difficulty to insert or remove the instrument from the cannula or imprecise motion. Affected

8mm Monopolar Curved Scissors (2018-10-23)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/68392r-eng.php

Nov 28, 2018 ... Identification number: RA-68392 Reason Affected products Affected products 8mm Monopolar Curved Scissors Reason Specific versions of the Monopolar Curved Scissor (MCS) instruments can become distorted at the tube extension during sterilization, resulting in difficulty to insert or remove the instrument from the cannula or imprecise motion. Affected products 8mm Monopolar

OriGen VV13F Reinforced Dual Lumen ECMO Catheters (2015-04-03)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2015/53173r-eng.php

..., Healthcare Professionals, Hospitals Identification number: RA-53173 Reason Affected products Recalled Products A. OriGen VV13F Reinforced Dual Lumen ECMO Catheters Reason The separation of the clear extension tube from the blue hub connection may result in massive blood loss from the patient and massive air entrainment into the ECMO circuit. Affected products

Pressure Monitoring Sets (2015-08-18)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2015/55202r-eng.php

... adaptor. The IV tubing lumen was blocked by the adaptor and restricted flow paths to extension tubes and pressure lines. Affected products A. Pressure Monitoring Set Lot or serial number 987950 0020223 0036750 Model or catalog number 2X3 43422A Companies Manufacturer Edwards Lifesciences LLC 1 Edwards Way Irvine UNITED STATES B. Pressure Monitoring Kit with VAMP

3T Design recalls Cervélo Bicycles with Aduro Aero Handlebars

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2014/37863r-eng.php

Feb 4, 2014 ... are black with red and white stripes. “P5” is on the seat tube, "Cervélo" is on the top tube and a large “é” is on the down tube in white lettering. The handlebars consist of four major components: a base bar, which attaches to the bike; a forward extension mount, which attaches to the base bar; forearm rests and forward extension bars, which attach to the forward

HEMODIALYSIS CATHETER SETS (2015-06-23)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2015/54624r-eng.php

Aug 11, 2015 ... Professionals, Hospitals Identification number: RA-54624 Reason Affected products Affected Products HEMO-CATH SILICONE DOUBLE LUMEN TEMPORARY ACCESS CATHETERS HEMO-CATH SILICONE DOUBLE LUMEN TEMPORARY ACCESS CATHETER SETS PEDIATRIC HEMO-CATH SILICONE DOUBLE LUMEN TEMPORARY ACCESS SILICON CATHETER SETS Reason Cracks in silicon extension tubing of hemodialysis catheters

Eppendorf MixMate Laboratory Plate and Tube Mixer

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2011/11816r-eng.php

Dec 18, 2012 ... request alternate formats by contacting us. Eppendorf MixMate Laboratory Plate and Tube Mixer Report a Concern Starting date: May 5, 2011 Posting date: May 5, 2011 Type of communication: Consumer Product Recall Subcategory: Household Items, Tools and Electrical Products Source of recall: Health Canada Audience: General Public (GP) Identification number: RA

2009 Felt Model  B12, B16, and  S32 Road Bicycles

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2010/13028r-eng.php

Dec 10, 2012 ... should do Affected products 2009 Felt Model B12, B16, and S32 Road Bicycles Product description This recall involves all 2009 Felt model B12, B16, and S32 road bicycles. 2009 Felt Model B12 - These bicycles are gloss silver/carbon and have carbon fiber frames with carbon fiber forks with aluminum steer tubes. 2009 Felt Model B16 - These bicycles are matte black

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