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Momcozy wearable breast pumps were sold in the Canadian market without the proper authorization (i.e., medical device licence [MDL]). Recall start date: January 28, 2023

In the course of internal quality controls, Draeger has noticed that some of their flex ventilation hoses have contaminations. Due to a deviation in the manufacturing process, components of the hose material remained as particles inside the hoses.…

As of January 19th, the company has received one incident report of a gas hose melting causing the table to catch fire in Canada, and no injuries have been reported.

The recalled products do not contain the intended levels of preservative which may lead to the growth of bacteria and other microorganisms during the product's shelf life and during manufacturing. People with healthy immune systems are usually not…

Specific lots have the potential for a broken sled vane component. A broken sled vane may cause the reload to misfire leading to non-functional staple line closure, transecting tissue without forming staples, and tissue hang-up. These conditions may…

Baxter Corportation is issuing a recall for certain lots of the Minicap. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals.  Recall start date: February 01, 2023

Affected lot exceeds concentration limit for N-nitrosodimethylamine (NDMA) at the 48-month stability testing timepoint.

Convatec is conducting a medical device recall for a specific lot of Aquacel® Ag foam adhesive 10cm x 10cm due to the visual contamination in the form of brown spots present on dressings. An internal investigation determined that the likely root cause…

During the investigation process of customer complaints, Lina has become aware of a safety issue in relation to the use of an obsolete version of an accompanying document. The use of an obsolete customer quick reference guide resulted in the incorrect…

Medline 3" walker wheels with glide caps can potentially come with a loose acorn nut that attaches the wheel to the leg. Health consequences include the chances of the wheel becoming loose and disconnecting resulting in an unstable condition of the…

Hologic has received a single report of a c-arm performing a significant unexpected movement during non-patient related use of the system. The investigation determined this event was due to a hardware component failure. Recall start date: January 16,…

Through ongoing internal testing, Baxter Corporation has observed isolated incident of over infusion on the Novum IQ LVP infusion pump during test runs at 0.1 ml/hr after 40 hours of continuous infusion within the 96-hour set change interval. Baxter…

Issue: This recall is for certain 4-point harnesses, manufactured by IMMI, that were sold as accessories by Can-Am dealers. This recall is not being conducted under the requirements of the Motor Vehicle Safety Act. Certain 4-point harnesses may be…

Issue: On a small number of fire trucks, there may be a defect in the rear axle drive pinion that could cause it to break. If this happens, the air brake line could be damaged and cause the parking brakes to apply suddenly. Note: This recall only…

Issue: On one fire truck, there could be a problem with circuit board for the electrical multiplex module (Weldon V-Mux Hercules HC 1.5 node). This could cause some vehicle systems not to work properly, including the headlamps and taillamps. Safety…