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When the Product is opened incorrectly by the front or smaller side during use, the front or smaller side of the product can fall and pose a potential injury hazard to the consumers. Furthermore, if the product is not anchored to the wall when in the…

Maquet S.A.S. /Getinge has received a customer complaint regarding a fall of a light system in an operating room in Hong Kong (no injuries reported). Tnvestigation into this event demonstrated that the recommendation of maintenance and service were not…

Smith Medical has issuing a recall of its Logical 3 Gang Manifold due to potential defect with the rotating   adaptor(rotator) which is incorporated as a component within the product. It was identified that the inner diameter of the device's o-ring…

Philips Respironics found during an internal review that the Evo product listed above had errors in their instructions for use (IFUs). Recall start date: November 20, 2023

When the Bugaboo Dragonfly Stroller is unfolded with the seat in "parent-facing" position and the backrest of the seat is unfolded directly into a horizontal position, rather than the fully upright position the seat backrest will not be properly secured…

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

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,…

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

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…

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…

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…