Health Canada · October 8, 2026
- Affected product
- Avantage Inserter Handles and Grippers
- Category
- Product recall
- Hazard
- It was identified while using the Avantage inserter handles and grippers during the implantation of the acetabular shell, that the acetabular shell may not consistently disengage from the gripper when the trigger is unlocked. As a result, the inserter handle…
Check affected Avantage Inserter Handles and Grippers identifiers →Health Canada · October 7, 2026
- Affected product
- GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive
- Category
- Product recall
- Hazard
- Gore has identified through quality control testing that some VIABAHN® devices were processed using equipment that was functioning outside of the validated range. This could potentially result in an incorrect bonding location of the distal tip onto the…
Check affected GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive identifiers →Health Canada · October 7, 2026
- Affected product
- Perma-Sharp Sutures
- Category
- Product recall
- Hazard
- Perma-sharp sutures are manufactured for Hu-Friedy by 2 manufacturers. 1. Surgical Specialties Corporation has cleared for the U.S. market & 2. Camark SA are authorized for the European Union, United Kingdom, Switzerland, & Israel. Products have same…
Check affected Perma-Sharp Sutures identifiers →Health Canada · October 6, 2026
- Affected product
- PMS-Carvedilol 25 mg Tablets: Out-of-specification (Impurity)
- Category
- Product recall
- Hazard
- The impurity, N-nitroso-carvedilol, may be out of specification in the affected lots.
Check affected PMS-Carvedilol 25 mg Tablets: Out-of-specification (Impurity) identifiers →Health Canada · October 6, 2026
- Affected product
- Fluoroplastic Vent Tube
- Category
- Product recall
- Hazard
- Vent tube devices across lot 0231048280 were identified to have been released to customers without undergoing sterilization. the issue is currently understood to originate from manufacturing (load preparation) and represents a fault condition: the product does…
Check affected Fluoroplastic Vent Tube identifiers →Health Canada · October 6, 2026
- Affected product
- Carvedilol 25 mg Tablets: Out-of-specification (Impurity)
- Category
- Product recall
- Hazard
- The impurity, N-nitroso-carvedilol, may be out of specification in the affected lots.
Check affected Carvedilol 25 mg Tablets: Out-of-specification (Impurity) identifiers →Health Canada · October 6, 2026
- Affected product
- FreeO2 Automated Oxygen Therapy Device Adult & Pediatric
- Category
- Product recall
- Hazard
- A battery reading error may occur when certain Freeo2 HW 1.2 devices are restarted following an upgrade from software version 1.2.X to 1.4.X. The error is immediately detectable, prevents the device from being returned to service and requires installation of a…
Check affected FreeO2 Automated Oxygen Therapy Device Adult & Pediatric identifiers →Health Canada · October 5, 2026
- Affected product
- PDP-DIPHENHYDRAMINE 25 MG CAPSULE: Out-of-specification (Impurity)
- Category
- Product recall
- Hazard
- The impurity, N-Nitroso-N-Desmethyl Diphenhydramine, is out of specification in the affected lots.
Check affected PDP-DIPHENHYDRAMINE 25 MG CAPSULE: Out-of-specification (Impurity) identifiers →Health Canada · October 5, 2026
- Affected product
- Lumify Ultrasound System
- Category
- Product recall
- Hazard
- due to reduced access to wi-fi/cellular. Philips has received reports that these erroneous re-registration events have prevented scanning in pre-hospital environments and delayed care to patients. These pre-hospital events occurred outside of wi-fi or cellular…
Check affected Lumify Ultrasound System identifiers →Health Canada · October 5, 2026
- Affected product
- Carvedilol 25 mg Tablets: Out-of-specification (Impurity)
- Category
- Product recall
- Hazard
- The impurity, N-nitroso-carvedilol, may be out of specification in the affected lots.
Check affected Carvedilol 25 mg Tablets: Out-of-specification (Impurity) identifiers →Health Canada · October 2, 2026
- Affected product
- Automated Impella® Controllers (AIC)
- Category
- Product recall
- Hazard
- patient populations, may lead to temporary inadequate hemodynamic support or a temporary loss of hemodynamic support. Hospital inventory may continue to be used to ensure continuity of care. Not all units are affected by this issue. Additional information…
Check affected Automated Impella® Controllers (AIC) identifiers →Health Canada · October 2, 2026
- Affected product
- Medline Single Sterile C-Section Drapes W/Incise
- Category
- Product recall
- Hazard
- Medline Industries, LP is issuing a correction notice for specific lot numbers of the Medline single sterile C-section drapes w/incise due to customer reports of C-section drapes being difficult to remove from patients, leaving adhesive residue on the…
Check affected Medline Single Sterile C-Section Drapes W/Incise identifiers →Health Canada · October 1, 2026
- Affected product
- Ethicon Nylon Suture
- Category
- Product recall
- Hazard
- Ethicon determined that some ETHILON™ Nylon Suture from the lot subject to this recall (removal) have needles that are distorted/twisted in the primary packaging. Up to 17% of the impacted lot may have the needle defect.
Check affected Ethicon Nylon Suture identifiers →Health Canada · October 1, 2026
- Affected product
- CareLink™ SmartSync™ Device Manager
- Category
- Product recall
- Hazard
- A complaint from the CareLink network reported a sudden decrease in the Remaining Longevity of a patient's Micra VR CIED from 3 years to 6 months following a remote transmission, which was later found to be incorrect. Analysis revealed a calculation issue in…
Check affected CareLink™ SmartSync™ Device Manager identifiers →Health Canada · October 1, 2026
- Affected product
- Medline Sterile Surgical Kits containing Medline C-Section Drape
- Category
- Product recall
- Hazard
- A recall correction notice for Medline Sterile Surgical Kits containing Medline C-Section Drape w/Incise is being issued due to reports of the drapes being difficult to remove from patients, leaving adhesive residue on their skin. In these cases, patients may…
Check affected Medline Sterile Surgical Kits containing Medline C-Section Drape identifiers →Health Canada · September 28, 2026
- Affected product
- PMS-FAMPRIDINE 10 mg Tablet: Affected lot may contain foreign
- Category
- Product recall
- Hazard
- Affected lot may contain foreign material particles.
Check affected PMS-FAMPRIDINE 10 mg Tablet: Affected lot may contain foreign identifiers →Health Canada · September 28, 2026
- Affected product
- OmniaSecure™ MRI SureScan™
- Category
- Product recall
- Hazard
- The model 3930M is a transvenous DF4 lead labelled for use in the RV and left bundle branch area (LBBA). It uses a fixed helix design, so the lead must be rotated as a whole for fixation. It's design transfers torque from the connector and lead body to the…
Check affected OmniaSecure™ MRI SureScan™ identifiers →Health Canada · September 25, 2026
- Affected product
- PERMA-HAND™ Silk Suture
- Category
- Product recall
- Hazard
- Ethicon determined that PERMA-HAND™ Silk Suture subject to this recall (removal) was incorrectly manufactured with an alcohol-based tubing fluid in the primary packaging. This tubing fluid is an isopropyl alcohol (IPA), diethylaminoethanol (DEAE), and sodium…
Check affected PERMA-HAND™ Silk Suture identifiers →Health Canada · September 25, 2026
- Affected product
- Limited number of Sarclisa single use vials may have been frozen
- Category
- Product recall
- Hazard
- Units of the affected lot may have been frozen during shipping. Only nine (9) units from the lot are being recalled from three (3) locations in Nova Scotia.
Check affected Limited number of Sarclisa single use vials may have been frozen identifiers →Health Canada · September 25, 2026
- Affected product
- Sanofi-Aventis Canada Inc. certain insulin pens and cartridges
- Category
- Product recall
- Hazard
- s are identified. What you should do Only a limited number of units within the listed lots are affected by this recall. Do not assume your product is affected solely because the lot number appears in the table. If your product is labelled with a lot number…
Check affected Sanofi-Aventis Canada Inc. certain insulin pens and cartridges identifiers →Health Canada · September 25, 2026
- Affected product
- Amplatzer™ Amulet™ Left Atrial Appendage Occluder
- Category
- Product recall
- Hazard
- The current Amulet™ IFU contains a contraindication against use "where placement of the device would interfere with any intracardiac or intravascular structures." Abbott is updating this contraindication to specifically identify the pulmonary artery as one of…
Check affected Amplatzer™ Amulet™ Left Atrial Appendage Occluder identifiers →Health Canada · September 24, 2026
- Affected product
- Apo-Semaglutide Injection : Incorrect dose display
- Category
- Product recall
- Hazard
- The affected lot may display a dose of 0.25 mg or 0.5 mg in the dose window and deliver one of these doses instead of the expected 1 mg dose.
Check affected Apo-Semaglutide Injection : Incorrect dose display identifiers →Health Canada · September 24, 2026
- Affected product
- Likorall™ Patient Lift Systems
- Category
- Product recall
- Hazard
- Baxter Corporation is issuing an urgent medical device correction for the Likorall™ ceiling-mounted overhead patient lift system due to a potential issue involving motor shaft breakage combined with reduced performance of the single fault safety (SFS) system.…
Check affected Likorall™ Patient Lift Systems identifiers →Health Canada · September 24, 2026
- Affected product
- InterStim™ Systems
- Category
- Product recall
- Hazard
- Medtronic has received 15 complaints involving the selection of an incompatible component based on the intended system configuration between 01-Jan-2020 through 12-Aug-2026. Use of an incompatible lead or percutaneous extension has resulted in a delay of…
Check affected InterStim™ Systems identifiers →Health Canada · September 21, 2026
- Affected product
- IMAAVY: Affected lots may contain glass particles
- Category
- Product recall
- Hazard
- Affected lots may contain glass particles.
Check affected IMAAVY: Affected lots may contain glass particles identifiers →Health Canada · September 18, 2026
- Affected product
- Counterfeit laser hair removal and therapy devices found in some
- Category
- Product recall
- Hazard
- s Last updated 2026-09-18 Summary Product Soprano diode laser hair removal systems and diode laser therapy systems Issue Medical devices Health products - Product safety Health products - Unauthorized product What to do Do not buy or use unauthorized medical…
Check affected Counterfeit laser hair removal and therapy devices found in some identifiers →Health Canada · September 17, 2026
- Affected product
- RAPICIDE™ PA High Level Disinfectant
- Category
- Product recall
- Hazard
- STERIS identified through customer complaints that a small number of RAPICIDE™ Part A bottles within certain lots may begin to bulge or expand over time. Part A is the active component of chemistry that creates peracetic acid, which may off-gas during the…
Check affected RAPICIDE™ PA High Level Disinfectant identifiers →Health Canada · September 17, 2026
- Affected product
- Philips Ingenia, Achieva and Intera MR Systems
- Category
- Product recall
- Hazard
- When exporting diffusion tensor imaging (DTI) scans from a Philips MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for…
Check affected Philips Ingenia, Achieva and Intera MR Systems identifiers →Health Canada · September 17, 2026
- Affected product
- Trinity Biotech Oxalate Reagent Kit
- Category
- Product recall
- Hazard
- Trinity Biotech is recalling Oxalate Reagent B, Product Code 591-2, Lot 2500711 due to performance variability resulting in negative bias and under-recovery of oxalate values, potentially causing falsely low patient results. Users should discontinue use,…
Check affected Trinity Biotech Oxalate Reagent Kit identifiers →Health Canada · September 16, 2026
- Affected product
- IntelliSpace Critical Care And Anesthesia
- Category
- Product recall
- Hazard
- In ICCA releases J.06.01 and J.06.02, calculations triggered by infusion-pump auto-charting may result in incorrect Intake Totals, Output Totals, Net Body Balance, Length of Stay (LOS) Balance, and related fluid-balance values.This issue applies only to…
Check affected IntelliSpace Critical Care And Anesthesia identifiers →Health Canada · September 16, 2026
- Affected product
- NDI Passive Spheres™
- Category
- Product recall
- Hazard
- The sphere manufacturer has identified variation in the reflective material used on a limited number of sterile passive sphere lots. The reflective material is the outer coating of the sphere that reflects infrared light from the optical tracking cameras,…
Check affected NDI Passive Spheres™ identifiers →Health Canada · September 16, 2026
- Affected product
- Platinum Naturals Easymulti Stress (men): Affected lots incorrectly
- Category
- Product recall
- Hazard
- Affected lots are labelled with the incorrect amount of a medicinal ingredient (Vitamin B6).
Check affected Platinum Naturals Easymulti Stress (men): Affected lots incorrectly identifiers →Health Canada · September 15, 2026
- Affected product
- Organika® Gummies: Foreign site not listed on site licence
- Category
- Product recall
- Hazard
- Affected lots were imported from a foreign manufacturing site not listed on the site licence.
Check affected Organika® Gummies: Foreign site not listed on site licence identifiers →Health Canada · September 14, 2026
- Affected product
- TZIELD (teplizumab) and the Viral Reactivation
- Category
- Product recall
- Hazard
- communication TZIELD (teplizumab) and the Risk of Viral Reactivation Last updated 2026-09-14 Summary Product TZIELD, teplizumab for injection, 2 mg per 2 mL (1 mg/mL) for intravenous infusion Issue Health products - New safety information Health products -…
Check affected TZIELD (teplizumab) and the Viral Reactivation identifiers →Health Canada · September 10, 2026
- Affected product
- Dxc 500i Clinical Analyzer and Dxc 500 AU Clinical Chemistry
- Category
- Product recall
- Hazard
- Beckman Coulter identified a software issue affecting DxC 500i and DxC 500 AU Analyzers when testing plasma samples. Following user configuration of a chemistry test to nondefault units, subsequent activation of a draft configuration in the system…
Check affected Dxc 500i Clinical Analyzer and Dxc 500 AU Clinical Chemistry identifiers →Health Canada · September 10, 2026
- Affected product
- Generic acetaminophen by Teva recalled because it may contain
- Category
- Product recall
- Hazard
- Teva Canada Limited is recalling one lot of the non-prescription drug Novo-Gesic Forte 500 mg (acetaminophen) due to the potential presence of phenolic resin or epoxy which, if ingested, may cause injury to the digestive system. The affected product was…
Check affected Generic acetaminophen by Teva recalled because it may contain identifiers →Health Canada · September 4, 2026
- Affected product
- Imager™ II Angiographic Catheter
- Category
- Medical device recalls
- Hazard
- of tip degradation and detachment. Additional information Details Original
Check affected Imager™ II Angiographic Catheter identifiers →Health Canada · September 4, 2026
- Affected product
- LIFEPAK ® 35 Monitor/Defibrillator
- Category
- Product recall
- Hazard
- During production of LP35, Stryker identified that certain printer and modem access port connectors may not have been fully seated within the rear housing assembly. As a result, the connectors may appear flush with or recessed relative to the retaining nut…
Check affected LIFEPAK ® 35 Monitor/Defibrillator identifiers →Health Canada · September 2, 2026
- Affected product
- LIFEPAK ® 35 Monitor/Defibrillator
- Category
- Product recall
- Hazard
- Stryker has identified an issue with the LP35 where the device does not display the message "CHECK RHYTHM / ECG Analysis Inconclusive" as intended when specific conditions are present simultaneously. The issue does not affect the display of "shock advised" or…
Check affected LIFEPAK ® 35 Monitor/Defibrillator identifiers →Health Canada · August 31, 2026
- Affected product
- JAMP Temozolomide: Out-of-Specification (Assay)
- Category
- Product recall
- Hazard
- The active ingredient (temozolomide) is out of specification in the affected lot.
Check affected JAMP Temozolomide: Out-of-Specification (Assay) identifiers →
