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The metal doll pin contains paint with lead levels exceeding Canadian regulations. The hoodie has drawstrings which is prohibited on children’s outerwear. As of June 2, 2023, the company has received no reports of incidents or injuries in Canada.

The concentration of Chlorhexidine Gluconate may be out of specification in the affected lots.

A textile defect was identified within the body of an Hemagard Knitted Bifurcated Vascular Graft.  This issue has been identified as lot # and serial # specific. Recall start date: June 2, 2023

There is the potential that an incorrect type of secondary latch could have been installed on the northeast (ne) and/or northwest (nw) bedside panels for certain Giraffe Omnibed Carestation devices (serial number specific). With the incorrect type of…

The affected products are being recalled from the marketplace due to possible norovirus contamination.

The affected product is being recalled from the marketplace because it may permit the growth of Clostridium botulinum.

The power loveseats, sofas, and recliners’ LED lighting feature inside the cup holder may fail after prolonged use, leading to overheating and risk of fire. As of May 30th, 2023, the company has received no reports of consumer incidents or injuries…

The recalled mirrors can detach from the frame, causing the mirror to fall, posing a laceration hazard to consumers. As of June 1, 2023, the company has received no reports of incidents in Canada, and no reports of injuries. In the United States, the…

The helmet straps may detach from the helmet causing the helmet to dislodge from the users head. During an accident, the user’s head may not be protected. As of March 1, 2023, the company has received no reports of incidents in Canada, and no…

The products do not meet the flammability requirements under the Children’s Sleepwear Regulations that can result in a burn hazard. As of May 3rd, 2023, the company has received no reports of incidents in Canada, and no reports of injuries. In the…

Beckman Coulter has confirmed that specific diluent lot numbers showed that conductivity, osmolality, and ph were out of manufacturing specifications. Quality control results may fail to flag for the affected parameters. Not all diluent containers within…

Based on an internal investigation, Integra Lifesciences has identified issues with in-process and finished goods endotoxin testing that may result in out of specification endotoxin results. Accordingly, we are recalling those products per the…

The update provides a network isolator for the lan connection, which must be installed in the Mira Max vf10 systems. The isolator is a measure of operator protection. Recall start date: May 29, 2023

Teleflex has initiated a voluntary recall due to reports of disconnection of the 15mm connector from the endotracheal tube (et tube) for the affected products. Recall start date: May 26, 2023

Stryker has identified that the base leg assembly may bend. Bent base leg assembly may result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lowering the cot, cot tip, or erratic or…