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Vyaire today announced an immediate global recall of the enFlow® Disposable Cartridges used with the enFlow® fluid warming system (part numbers 980200EU, 980202EU). Vyaire’s decision to initiate an URGENT RECALL NOTIFICATION was based on recently conducted internal testing which has indicated that there is the potential to elude aluminum from the enFlow® Disposable Cartridge during intravenous warming therapy with fluid and blood solutions. This Global Recall is being conducted based on the potential patient safety risk associated with aluminium toxicity. Vyaire has received zero (0) customer complaints to-date related to the signs, symptoms or complications associated with aluminum toxicity subsequent to patient use.

The Quality team at Trudell Medical Marketing Ltd. will immediately begin to action this recall and all customers will be notified with complete details. Should you have any questions, please contact your Trudell Territory Manager or customer service at

Vyaire Medical, a global leader in respiratory care and partner of TMML, has acquired Acutronic Medical Systems and, separately, entered into a definitive agreement to acquire imtmedical. These acquisitions will bring new and innovative ventilation options to the Canadian healthcare market.

Post-operative pulmonary complications (PPCs) are a major burden to the healthcare system. A new real-world study published in Pulmonary Therapy, indicates significant reductions in costs when using the Aerobika* oscillating positive expiratory pressure (OPEP) device in the postoperative care setting.1

We are excited to introduce the Parker Medical line of intubation products from Salter Labs.  This includes the Flex-Tip™ Tracheal Tube, ThinCuff® Tracheal Tube, Flex-Tip® Nasopharyngeal Airways, Intubating Stylets and the Parker Double-Lumen Endobronchial Tubes.

The CarboTrack™ device was specifically designed to facilitate compliance with ESA standards for capnography for non-intubated patients. It serves a very broad range of target airways including but not limited to supplemental oxygen face masks, oropharyngeal airways, and bite blocks. CarboTrack™ aims to replace the widespread practice of jerry-rigging equipment in the operating room with the first FDA listed and CE marked device for this purpose.