Health Canada · August 27, 2026
- Affected product
- Apo-Semaglutide Injection : Incorrect dose display
- Category
- Product recall
- Hazard
- The affected lot may display a 2 mg dose in the dose window and deliver a 2 mg dose instead of the expected 0.25 mg or 0.5 mg dose.
Check affected Apo-Semaglutide Injection : Incorrect dose display identifiers →Health Canada · August 27, 2026
- Affected product
- pro+ Flat Deck Wide W/O X-Ray
- Category
- Product recall
- Hazard
- The UDI label for model p7924a13 incorrectly states the product description as "Pro+ 40 MRS surface with x-ray" instead of the actual configuration, which is "Pro+ 36 MRS surface." Model p7924a13 should be used with 36" width bed frames and not 40" width bed…
Check affected pro+ Flat Deck Wide W/O X-Ray identifiers →Health Canada · August 26, 2026
- Affected product
- Med-Rx Medication/Primary Solution Administration Kit
- Category
- Product recall
- Hazard
- CHS was notified by ICU Medical Canada that they are conducting a recall of certain IV sets as discoloration may be present in the drip chamber of the IV sets. ICU Medical IV Tubing Dets with a drip chamber that are within their expiration date are impacted.…
Check affected Med-Rx Medication/Primary Solution Administration Kit identifiers →Health Canada · August 26, 2026
- Affected product
- CARESCAPE Central Station
- Category
- Product recall
- Hazard
- GE Healthcare has become aware that the CARESCAPE Central Station (CSCS) v3.0.x may not resume patient monitoring for at least 3 minutes following a system restart.
Check affected CARESCAPE Central Station identifiers →Health Canada · August 26, 2026
- Affected product
- BIOFIRE® Joint Infection Panel – 30 Pack
- Category
- Product recall
- Hazard
- Beginning April 5, 2026, elevated rates of KPC unexpected positives were observed in reagent final QC testing of the BIOFIRE® FILMARRAY® Pneumonia Panel, BIOFIRE® FILMARRAY® Pneumonia Panel Plus, and BIOFIRE® Joint Infection Panel, including in passing product…
Check affected BIOFIRE® Joint Infection Panel – 30 Pack identifiers →Health Canada · August 26, 2026
- Affected product
- Maquet Percutaneous Insertion Kit and Dilator Sets
- Category
- Product recall
- Hazard
- The manufacturer became aware of this issue during retrospective review of historical packaging verification documentation. It was identified that there have been failures in sterile barrier integrity verification testing. As these failures were not previously…
Check affected Maquet Percutaneous Insertion Kit and Dilator Sets identifiers →Health Canada · August 25, 2026
- Affected product
- Twins Herbal Products: Undeclared prescription drug (sildenafil)
- Category
- Product recall
- Hazard
- Products sold without market authorization (DIN) in Canada. Products contain undeclared sildenafil that is listed on the prescription drug list.
Check affected Twins Herbal Products: Undeclared prescription drug (sildenafil) identifiers →Health Canada · August 24, 2026
- Affected product
- Importation of South Korean-Authorized BONKY Injection, 1 mcg/mL
- Category
- Product recall
- Hazard
- communication Importation of South Korean-Authorized BONKY Injection, 1 mcg/mL Calcitriol, due to the Current Shortage of Canadian-Authorized Calcitriol Injection USP, 1 mcg/mL Last updated 2026-08-24 Summary Product BONKY Injection, 1 mcg/mL Calcitriol Issue…
Check affected Importation of South Korean-Authorized BONKY Injection, 1 mcg/mL identifiers →Health Canada · August 21, 2026
- Affected product
- ForeSight™ Oximeter Cable
- Category
- Product recall
- Hazard
- This recall is regarding inaccurate StO2 readings from the HEMFSM10 ForeSight™ Oximeter Cable due to mispositioning of the sensor cables. Edwards has identified that during manufacturing, the laterality identification labels may be missing or inaccurately…
Check affected ForeSight™ Oximeter Cable identifiers →Health Canada · August 21, 2026
- Affected product
- Aisys™ CS² and Carestation™
- Category
- Product recall
- Hazard
- The Aisys™ Carestation™ Anesthesia System, Aisys™ CS² and Aisys™ CS² with Et Control, containing certain electronic gas mixer assemblies, can automatically transition to Alternate O2 Control.
Check affected Aisys™ CS² and Carestation™ identifiers →Health Canada · August 20, 2026
- Affected product
- Theragun PRO
- Category
- Product recall
- Hazard
- of a potential thermal event. Consumers should stop using the charger immediately and
Check affected Theragun PRO identifiers →Health Canada · August 19, 2026
- Affected product
- CISATRACURIUM BESYLATE INJECTION USP MULTIDOSE: The level of the
- Category
- Product recall
- Hazard
- The level of the degradation product Benzaldehyde may be out of specification in the affected lots.
Check affected CISATRACURIUM BESYLATE INJECTION USP MULTIDOSE: The level of the identifiers →Health Canada · August 19, 2026
- Affected product
- Embosphere® Microspheres-Syringe
- Category
- Medical device recalls
- Hazard
- (s), use of the
Check affected Embosphere® Microspheres-Syringe identifiers →Health Canada · August 19, 2026
- Affected product
- SPECTRALIS® with Flex Module
- Category
- Product recall
- Hazard
- There is a possibility that the castor wheels of the Flex stand are not properly attached. The wheels may come loose. As a result, the Flex stand may tip over. Users shall schedule a service appointment as soon as possible so that the castor fastenings can be…
Check affected SPECTRALIS® with Flex Module identifiers →Health Canada · August 18, 2026
- Affected product
- Unauthorized drugs seized from Rabais 4Saisons Inc. in Montreal, QC
- Category
- Product recall
- Hazard
- s - Canada.ca Skip to main content Skip to "About government" Language selection French fr Search Search Website Search You are here Canada.ca Health Recalls and safety alerts Recalls and safety alerts Public advisory Unauthorized drugs seized from Rabais…
Check affected Unauthorized drugs seized from Rabais 4Saisons Inc. in Montreal, QC identifiers →Health Canada · August 17, 2026
- Affected product
- Lactated Ringer's Injection USP: Presence of Particulate Matter
- Category
- Product recall
- Hazard
- Presence of particulate matter in affected lot
Check affected Lactated Ringer's Injection USP: Presence of Particulate Matter identifiers →Health Canada · August 15, 2026
- Affected product
- Two lots of Teva-Pregabalin 150 mg capsules recalled
- Category
- Product recall
- Hazard
- Teva Canada Ltd. is recalling two lots of Teva-Pregabalin 150 mg capsules after routine testing identified that some capsules may be contaminated with the drug sertraline. Patients with a hypersensitivity or allergy to sertraline could experience side effects…
Check affected Two lots of Teva-Pregabalin 150 mg capsules recalled identifiers →Health Canada · August 14, 2026
- Affected product
- Endotracheal Tube, Cuffed
- Category
- Product recall
- Hazard
- The 6FR suction catheter could not pass smoothly through the 2.5mm sizes of cuffed tracheal tube. This may lead to reintubations if the airway is unable to be suctioned.To date, there have been two complaints reported from united states customers where one…
Check affected Endotracheal Tube, Cuffed identifiers →Health Canada · August 14, 2026
- Affected product
- Orthopaedic Implant Components
- Category
- Medical device recalls
- Hazard
- Stryker has become aware that the devices listed in the Customer Letter were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five (5) years. Industry guidance for storage duration of UHMWPE raw material used…
Check affected Orthopaedic Implant Components identifiers →Health Canada · August 13, 2026
- Affected product
- Portrait Core Services Cssxb
- Category
- Product recall
- Hazard
- GE HealthCare has become aware that during a service event to update Portrait Core Services software at a facility, patients who are monitored on Portrait Mobile devices can be discharged from the Portrait monitoring system.
Check affected Portrait Core Services Cssxb identifiers →Health Canada · August 13, 2026
- Affected product
- IV Tubing Set Drip Chambers
- Category
- Product recall
- Hazard
- ICU Medical received reports of discoloration observed in the drip chambers of certain IV tubing sets.
Check affected IV Tubing Set Drip Chambers identifiers →Health Canada · August 12, 2026
- Affected product
- pms-IRBESARTAN: Affected lot may contain pms-IRBESARTAN/HCTZ
- Category
- Product recall
- Hazard
- The affected lot may contain pms-IRBESARTAN/HCTZ 150/12.5 mg tablets.
Check affected pms-IRBESARTAN: Affected lot may contain pms-IRBESARTAN/HCTZ identifiers →Health Canada · August 12, 2026
- Affected product
- Unauthorized injectable health products sold online and seized from
- Category
- Product recall
- Hazard
- s - Canada.ca Skip to main content Skip to "About government" Language selection French fr Search Search Website Search You are here Canada.ca Health Recalls and safety alerts Recalls and safety alerts Public advisory Unauthorized injectable health products…
Check affected Unauthorized injectable health products sold online and seized from identifiers →Health Canada · August 11, 2026
- Affected product
- Semaglutide Injection: Incorrect Pen in Package
- Category
- Product recall
- Hazard
- The affected lot contains a 4 mg pen but is labelled as a 2 mg pen.
Check affected Semaglutide Injection: Incorrect Pen in Package identifiers →Health Canada · August 11, 2026
- Affected product
- Omni-Tract Surgical Retractor System
- Category
- Product recall
- Hazard
- Integra Lifesciences is issuing a correction to the Integra® Omni-Tract® Surgical Retractor System - existing Instructions For Use (IFU) related to prevacuum sterilization dry time requirements, to ensure the Omni-Tract® devices and components are properly…
Check affected Omni-Tract Surgical Retractor System identifiers →Health Canada · August 7, 2026
- Affected product
- TEVA-ECTOSONE 0.1% Cream; Affected lot may be missing lot number and
- Category
- Product recall
- Hazard
- Affected lot may be missing the lot number and expiry date on the label.
Check affected TEVA-ECTOSONE 0.1% Cream; Affected lot may be missing lot number and identifiers →Health Canada · August 7, 2026
- Affected product
- Adequan I.M: Presence of particulate matter
- Category
- Product recall
- Hazard
- Presence of particulate matter in affected lot.
Check affected Adequan I.M: Presence of particulate matter identifiers →Health Canada · August 7, 2026
- Affected product
- Bravo - Capsule Delivery System
- Category
- Product recall
- Hazard
- s associated with this issue include patient aspiration/inhalation, perforation of esophagus, obstruction of the airway, hemorrhage/blood loss/bleeding, laceration of the esophagus, a delay in diagnosis, and foreign bodies remaining in the patient. Lots with…
Check affected Bravo - Capsule Delivery System identifiers →Health Canada · August 6, 2026
- Affected product
- One lot of New Roots Herbal Probiotic Intensity recalled incorrect
- Category
- Product recall
- Hazard
- s to people with a severe dairy allergy. Although the labelling issue affects only the 30-count bottles, the company is recalling the entire lot, which also includes 60-count bottles. The recalled lot was distributed starting in October 2025. People with…
Check affected One lot of New Roots Herbal Probiotic Intensity recalled incorrect identifiers →