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UPDATE (2022-07-27): Update on Philips Respironics recall of several models of CPAP and BiLevel PAP machines and mechanical ventilators Health Canada is providing an update on the progress of Philips Respironics’ (Philips) recall of several models of…

On 03/17/2022, a Stryker spine operator packaging non-sterile Yukon Straight Rods from finished goods inventory discovered a Yukon Straight Rod 120 mm (cat#7601-540120, lot# pcmw) with orange and white discoloration on the surface of the device.…

The recall activities are being conducted due to several temperature excursions on inbound shipment to Canada.  According, to the assessment by the manufacturer, Anteis S.A, no data is available for Belotero products after repeated freezing and…

Reports of products having torn corrugated breathing tube.   - Should a tear be detected before use, a delay may be experienced while another product is located.   - Should a tear be detected during use, this may result in a leak and…

The ook snow ALL when used with motorized wheel system, and bearing the option number OL2000200WG may continue to move forward even after the trigger was released. Recall start date: Apr 11, 2022

Ortho Clinical Diagnostics received complaints in which customers obtained unexpected results on their Ortho Vision Analyzer. upon further investigation, Ortho confirmed that incorrect utilization of the "assign to position" feature by physically placing…

The proximal marker on devices from these lots may separate from the device. A dislodged marker may require additional intervention, including unplanned additional coronary intervention, or surgery. To date Abbott has received 5 complaints related to…

The Universal Plus™ Laparoscopic Electrodes devices are sold as single use, sterile devices. Conmed received reports that the tip of the electrode could detach during use. Recall start date: Apr 19, 2022

The battery wiring harness on the effected TDX SP2 narrow base wheelchairs may become disconnected during shipment from the factory or during wheelchair use traversing large obstacles or after a jolt or impact to the wheelchair. The disconnection of the…

Ortho Clinical Diagnostics has observed an increase in complaints, and confirmed observed imprecision, for low-level quality control (QC) and patient samples at the low end of the measuring (reportable) range when using Vitros FSH, LH and PROL reagent.…

During a routine inspection Medtronic noted there was damage to the sterile pouch that contains the In.Pact Admiral Catheters. Upon investigation, there had been a change implemented to one manufacturing line which may cause pouch damage. All batches…

The purpose of this notification is to inform you of a product correction for the Alinity I Homocysteine Reagent Kits listed in the letter. Abbott has identified that some reagent kits produce suboptimal calibrations resulting in a downward shift of…

A review of customer feedback on Vessel Sealer Extend (VSE) PN480422 was done to determine rate of harm (bleeding harms) due to insufficient sealing.  This action taken to notify users to reduce potential harms. Recall start date: Mar 3, 2022

Devices from these lots may exhibit leaks and/or a loose connection at the rotating luer assembly or stopcock connection, which could lead to air ingress under vacuum. Analysis indicates an estimated rate of occurrence of air ingress associated with the…

HS1/onsite/home AED pads (pn: m5071a, m5072a) have been observed to experience gel separation from the foam/tin backing when peeled from the yellow plastic liner. The gel may fold onto itself resulting in reduced surface area of gel on the pad, or it may…