JAMP Temozolomide Capsules Recalled for Assay Defect: Health Canada
JAMP Temozolomide by JAMP Pharma Corporation
The active ingredient temozolomide was found to be out of specification during assay testing, meaning capsules…
Undeclared Fluoxetine, DNP Trigger Recall of Lipofit Extreme Fat Burner 2.0
Lipofit Extreme Fat Burner 2.0 by Lipofit
The AM tablets contained undeclared fluoxetine, a prescription antidepressant, while the PM tablets contained undeclared 2,4-dinitrophenol…
Health Canada Recalls Carestation 850 Anesthesia Systems Over Shutdown Risk
Carestation 850 by Datex-Ohmeda, Inc.
The Carestation 850 and 850C anesthesia systems can shut down unexpectedly when AC mains power is…
Zinc Oxide Particulate Risk Triggers B. Braun Saline Recall 2026
0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB Container by B. Braun
Testing found particulate matter identified as zinc oxide inside the saline containers. Administering the contaminated product…
Health Canada Recalls Cardinal Health Gynaecology, Endoscopy Packs 2026
Cardinal Health Gynaecology Robotics and Endoscopy Packs by Cardinal Health
The recalled packs contain a StrykeFlow PS handpiece component linked to an increased number of complaints…
Automated Impella Controller Recalled Over Purge Flag Failure: Health Canada
Automated Impella Controller (AIC) by Abiomed Inc.
A failing purge flag component can prevent the controller from correctly recognizing the purge cassette, most…
Poisoning Risk Prompts Recall of MD Wipe Outz Numbing Tattoo Wipes 2026
MD Wipe Outz Numbing Tattoo Wipes by Diamond Wipes International, Inc. / MD Wipe Outz
The wipes contain lidocaine, a topical anesthetic that by law must be sold in child-resistant packaging.…
Med-Rx IV Kits Recalled Over Discoloration in Drip Chamber: Health Canada
Med-Rx Medication/Primary Solution Administration Kit by Canadian Hospital Specialties Ltd. (CHS)
Discoloration has been found in the drip chamber of the IV sets used in these administration…
Health Canada Recalls BIOFIRE Joint Infection Panel Over False Positives
BIOFIRE® Joint Infection Panel – 30 Pack by Biofire Diagnostics, LLC.
Affected lots can produce false positive results for KPC, a gene linked to carbapenemase-producing organisms, due…
GE CARESCAPE Central Station Recalled Over Patient Monitoring Delay 2026
CARESCAPE Central Station by Ge Medical Systems Information Technologies Inc. (GE Healthcare)
The CARESCAPE Central Station (CSCS) v3.0.x may fail to resume patient monitoring for at least 3…
Two Lots of Baxter Sodium Chloride Injection Recalled Over Fiberglass Risk
0.9% Sodium Chloride Injection, USP, 500 mL VIAFLEX Plastic Container by Baxter
Intravenous administration of solution containing fiberglass particulate matter may cause blockage and clotting in blood vessels,…
Health Canada Recalls Cynosure DermaV Laser System Over Burn Risk
Cyanosure DermaV Laser System by Cynosure Lutronic Technology Corporation
Spark and loud noise events during vascular laser treatment at the 1064 nm wavelength, particularly at…
Fiberglass Particles Prompt Baxter Recall of Anticoagulant Solution 2026
Anticoagulant Sodium Citrate Solution USP, 250 mL VIAFLEX Plastic Container by Baxter
The solution may contain fiberglass particulate matter. If not caught by in-line filtration during apheresis use,…
Stainless Steel Particle Risk Prompts Baxter Dextrose Injection Recall 2026
70% Dextrose Injection, USP in 2000 mL VIAFLEX Plastic Container by Baxter
The recalled solution may contain stainless steel particulate matter, which if administered intravenously can cause blockage…
Sterility Failures Trigger Recall of Maquet Insertion Kits: Health Canada
Percutaneous Insertion Kit and Dilator Sets by Maquet Cardiopulmonary GmbH
Packaging used for the Percutaneous Insertion Kit and Dilator Sets may not consistently maintain sterile barrier…
Undeclared Sildenafil Prompts Recall of Twins Herbal Products 2026
Twins Herbal Idakole and Twins Herbal Pelorie by Twins Herbal
The products contain undeclared sildenafil, a prescription-only drug that can dangerously interact with nitrate medications used…
Health Canada Issues Type I Recall of Dräger VentStar Neo Resuscitation Devices
VentStar® Resus Neo and VentStar® Resuscitaire by Dräger (Draegerwerk AG & Co. KGaA)
Users have found obvious cracks in the breathing hose of the VentStar Resus Neo and VentStar…
Health Canada Authorizes South Korean BONKY Calcitriol Injection Import 2026
BONKY Injection, 1 mcg/mL Calcitriol by BONKY (YuYu Pharma Inc.)
The imported ampoule label warns that glass fragments may enter the solution when the ampoule is…
Superpotency Risk Triggers Vitruvias Thyroid Tablets Recall 2026
Thyroid Tablets, USP 30 mg by Vitruvias Therapeutics
Consumption of superpotent thyroid tablets can cause hyperthyroidism, including weight loss, heat intolerance, fatigue, nervousness, muscle…
ForeSight Oximeter Cable Recalled Over Mislabeled Sensors: Health Canada
ForeSight™ Oximeter Cable by Edwards Lifesciences LLC
Mislabeled sensor cables may cause the monitor to display swapped left-and-right StO2 (tissue oxygen saturation) readings.…