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 5 minutes ago
CanadaMequ A/S ºM Warmer Leakage
A misplaced seal may cause leakage internally in the ºM Warmer device.
Two lots of Omnitrope injectable human growth hormone recalled due to cracked cartridges
Sandoz Canada Inc.Alice Le System - Sleepware Software
Philips Respironics has become aware of a compliance issue with Sleepware G3 versions 4.0.0.0 and above, where the original 4.0 update was not licensed appropriately in…Allura Xper FD10
Philips has identified through customer complaints that, during certain repair or service actions, Hard Disk Drives (HDD) with different performance characteristics…TAVNEOS (avacopan) and Health Canada’s Review of Data Integrity Concerns
Health Canada is reviewing significant concerns regarding the data integrity of the pivotal ADVOCATE trial, which served as the primary efficacy study supporting the…JAMP Chlorthalidone 12.5 mg tablet: Out of specification (Dissolution)
The dissolution may be out of specification in the affected lot.Hotline IV Fluid Warmer System & Accessories
ICU Medical became aware of an increased likelihood of leakage in specific lots of L-70 Hotline Fluid Warming sets due to potentially inadequate solvent application at…Urinary Catheter Trays containing Cliniclean Pericare Wipes
Based on customer feedback, BD has identified that the Cliniclean Pericare Wipes provided within urinary catheter trays may be potentially contaminated with a lubricant…Intramedullary Bone Saw Blade Assembly
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Sawblade Assembly due to potential sterile barrier packaging…Hybrid Hydrophilic Microguidewire
Performance variability affecting the hydrophilic coating of Hybrid007 guidewires in specific lots may increase friction during microcatheter navigation.DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae
Beginning in April 2026, complaints were received regarding pinhole leaks in the wire-wound body of 22 Fr EOPA™ elongated one piece arterial cannulae and EOPA 3D™…Omni-Tract Surgical Retractor System
Integra Lifesciences is issuing a correction to the Integra® Omni-Tract® Surgical Retractor System - existing Instructions For Use (IFU) related to prevacuum…NephroMax High Pressure Nephrostomy Balloon Catheter
Boston Scientific is notifying you that the renal sheath for certain NephroMax™ high pressure nephrostomy balloon catheters may be packaged in a reversed orientation.Fludeoxyglucose (18F) Injection; Cracked vial
Fludeoxyglucose (18F) vial containing 24.80 mL (30.23 GBq of the product) used to administered the drug to the patients was found to be broken at the bottom.LIFECODES LSA Class II
Werfen has identified that two beads within the LIFECODES LSA class II assay kit(s) may present different DQB1 specificities than previously understood: • Bead 42 /…WASPLab
Copan WASP SRL is performing a medical device product correction related to the WASPLab product.Glidesheath Slender® Introducer Sheath
Through post-market surveillance, we have received complaints for the guidewire not being able to pass through the needle.AirSeal Access Port With Blunt Obturator and AirSeal Access Port With Optical Obturator
Complaint review identified a prior manufacturing process update that may cause erroneous overpressure alerts under certain conditions, potentially leading to loss of…RAPIDLab® 348EX System
Siemens Healthcare is informing affected customers that a software-related behavior identified in the RAPIDLab® 348EX System associated with the calcium ion…Abiomed Introducer Kits with Impella Heart Pumps
Abiomed has initiated a voluntary medical device recall (correction) for all currently distributed Introducer kits that are used with Impella heart pumps to notify…Remifentanil hydrochloride for injection; Out of specification (Assay & Impurity)
The assay and impurity is out of specification in the affected lots.Spiriva Capsules ; Out-of-specification (uniformity of delivered dose)
The affected lot may not consistently provide the intended dose of medication with each use.Infinion™ CX Contact Lead Kit
Boston Scientific is initiating a voluntary removal of unused Infinion™ CX Leads as part of the planned transition to the next generation lead (Infinion Pro).A little guidance
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