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Health Canada's compliance verification program has determined that one lot the product (Lot Number E20A139R), does not meet the requirements of the Consumer Chemicals and Containers Regulations, 2001 (CCCR, 2001) in Canada. Specifically,…

Potential for a small open channel in the lift and peel aluminum seal resulting in a compromised sterile barrier, potential for a lack of sterility assurance. Recall start date: November 13, 2023

Stryker received one (1) complaint for a LITe Decompression Tube Snake Arm that did not fit on to the arm post shaft that mounts to the hospital bed. Subsequent investigation determined a portion of one lot of the LITe Decompression Tube Snake Arm was…

When processing specific patient plasma specimens with the Aptima® CMV Quant Assay, a ML2 error flag may occur, which will invalidate specimens within the assay run. Recall start date: November 20, 2023

During an evaluation of user implementation of the instructions for use related to the reprocessing of the LTF-S190-5 videoscope, Olympus observed deviations from the following reprocessing steps detailed in the respective reprocessing manual…

The affected product is being recalled from the marketplace due to possible Listeria monocytogenes contamination.

An internal screw could drop between the cover rib and the cell printed circuit board and cause a short circuit, posing a fire hazard. As of November 7, 2023, the company has received no reports of incidents in Canada, and no reports of injuries. In…

The recalled product does not meet the labelling requirements and the child-resistant packaging requirements of the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act. The lack of appropriate labelling and…

Upon insertion of a new (unused) Ligasure™ device, the Valleylab™ FT10 energy platform running software versions 4.0.1, 4.0.2 and 4.0.3 may erroneously indicate that the Ligasure™ device was used previously. When this occurs, the energy platform will…

Ambu has received information on two incidents where Ambu® aView™ 2 Advance caught fire when mounted on the vesa holder of the aCart™ compact, due to incorrect length screws used penetrating the lithium-ion battery of the device. Investigations have…

Medtronic recently identified that if the Synchromed II Pump switches into telemetry mode due to electromagnetic interference (EMI) from an MRI scan, while the pump is sounding an alarm, the pump will not resume drug delivery after leaving the MRI…

Issue: On certain electric light utility vehicles, a problem with the lithium battery system could cause a fire, even while parked with the ignition off. Note: For the Hauler model, only the Hauler Pro and Hauler Pro X Elite models are affected by…

Issue: On certain vehicles, a problem with the steering control module could cause a turn signal not to turn off after making a turn or changing lanes. This problem could also cause the high beams to turn on when a turn signal is activated, or a turn…

Issue: On a small number of vehicles, the brake pedal assembly may not have been manufactured properly. As a result, the brake pedal could loosen and cause reduced braking or a loss of brakes. Safety Risk: Reduced braking or a loss of brakes can…

Issue: On certain F-150 Lightning (electric) trucks, a software problem could cause the electronic stability control (ESC) system not to return back to the default setting when the vehicle is started. Canadian regulations require the stability control…