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Results of post market surveillance revealed that under certain circumstances the room configuration parameters of the system are set to default values. If these values are larger than the actual room dimensions, a collision with the ceiling or wall…

Sanders brand Dark Chocolate Sea Salt Caramels recalled due to pieces of plastic. The recalled product has been sold in Ontario, Quebec, New Brunswick, Nova Scotia and Newfoundland and Labrador.

Sanders brand Dark Chocolate Sea Salt Caramels recalled due to pieces of plastic. The recalled product has been sold in New Brunswick, Ontario and Quebec.

Siemens Healthcare is informing customers with a preventive measure to exclude any potential risk of patient injury caused the footrest detaching from the patient table during an examination. Recall start date: December 15, 2022

Siemens Healthcare Diagnostics Inc. has confirmed an issue through complaint investigation. The issue has the potential to affect the recovery of po2 in quality control (qc) at elevation with barometric pressures <730 mmhg on epoc sensor configuration…

Teleflex has initiated a voluntary field safety corrective action due to reports of pilot balloon non-inflation or cuff non-deflation. In the event of pilot balloon non-inflation, there is a potential risk of injury to the patient as the pilot balloon no…

Loop Mission brand Probiotic Soda products recalled due to possible spoilage. The recalled products were sold in Ontario and Quebec.

The affected product is being recalled from the marketplace due to possible Listeria contamination. The recalled product may have been sold by various retailers, either clerk-served or in smaller packages, with or without a label that may not bear the…

Emergent received 3 complaints from customers between 18 Oct 2022 - 15 Nov 2022 related to leaking packets. Product in leaking packets may not perform as effectively as intended.  Recall start date: November 24, 2022

The concentration of the medicinal ingredient, sodium fluoride, is out of specification in the affected lot.

Medline packs contain 3M's Steri-drape, which are recalled due to the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product unusable. Recall start date: November 11, 2022

Some electrode pads used with the hs1/onsite/home AED 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.…

Affected lot may result in a false negative for skin test (peanut allergy).

Product sterility may be compromised in the affected lot.

The affected product is being recalled from the marketplace due to high levels of copper. The recalled product has been sold in British Columbia, Alberta, and online. It also may have been distributed in other provinces and territories.