Medicine, medical device and cosmetics recalls in Canada
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in Canada, newest first.
662 recalls, newest first · Checked 14 minutes ago
CanadaHeartSine® Samaritan® PAD SAM 350P/SAM 360P/SAM 500P
Stryker has identified a limited number of HeartSine samaritan PAD devices that were distributed without the required maintenance supplement.DCA Vantage® HbA1c (DX Claim)
Siemens Healthineers has confirmed through customer complaint investigation and internal testing that delamination of the buffer pull-tab may occur in a small subset of…HeartSine® Samaritan® PAD SAM 350P/SAM 360P/SAM 500P - Membrane Tail
Stryker has recently identified an issue with the membrane tail, an internal component, which could cause an intermittent fault.Cardinal Health - Presource® Kits Containing the Ritmed® Neurological Sponges
Cardinal Health was recently informed of a medical device recall from MEDICOM concerning the Ritmed® Neurological Sponges referenced.Shimadzu X-ray High Voltage Generators
Shimadzu Corporation has identified a potential issue in the X-ray High Voltage Generator.Atellica® CH Urine Albumin (UAlb)
Siemens Healthineers has confirmed, through the investigation of customer complaints, the potential for the following issues associated with processing Atellica CH…ER-Spec Single-Use Vaginal Speculum with LED Light Source
Units from specific lots of the ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small, may exhibit a plastic burr on the proximal plastic blade, near the…Merge PACS
Merge PACS Dynamic Thumbnail Refresh feature may cause thumbnails from a previously opened patient study to display in the Thumbnail Bar of a different patient's study.4K UHD LCD Monitor
Olympus determined that the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities if using one of those connectors.V-Loc™ 90 and 180 Suture Products
On 29-Jan-2026 during a quality inspection at a manufacturing site, a V-Loc 180 unit was found with a hole in the breather pouch on the Tyvek side.SEMA 3
When an ECG is aquired with DEFIGARD Touch 7 or ARGUS PRO LifeCare 3 with the newest software, there might be a discrepancy between the aquiring device and SEMA.StrykeFlow PS and AHTO
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.Philips Allura Xper FD series
Philips has identified a potential safety issue affecting Allura R8.2 systems equipped with a AD7x patient table type potentially leading to loss of geometry movements.Cardiac Workstation
The cardiac workstation can intermittently provide inaccurate data related to the patient's native heart rate.Leoni Plus
An electronic component may overheat internally.Presource ®Kits containing Teleflex Pilling® Wecksorb Neurosponge
Cardinal Health was recently informed of a medical device recall from Teleflex concerning the Pilling® Wecksorb Neurosponge referenced.CTP - Tubing sets
The manufacturer became aware of this issue due to six customer complaint reports.Supernova and Supreme Nicotine Film and Pouches Recall; No market authorization
Product sold without market authorization (DIN or NPN) in Canada.Solar™ GI
Under extended clinical use conditions (e.g., long-duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing…BD ChloraPrep™ Clear - 1mL Applicator: Product sterility
Product sterility could be compromised in affected lots.Oribe Serene Scalp Densifying Shampoo; Presence of bacterial contamination
Affected lots may contain the presence of bacterial contamination (pluralibacter gergoviae).Apo-Tiotropium Capsules; Out-of-specification (particle size)
The particle size did not meet the specifications in the affected lots.Phantom® Hindfoot TTC/TC Ball Tipped Guide Rod
Zimmer Biomet Canada on behalf of Paragon 28, Inc.A little guidance
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