BD MaxPlus Connector Minibore Extension Set Recall 2026

Health Canada has issued a Type I health product recall for the BD MaxPlus Connector Minibore Extension Set, a medical device used in healthcare settings. The recall, identified under reference number RA-82228, was initiated by BD Switzerland Sarl on June 17, 2026, following the discovery of a sterilization failure that may have left devices non-sterile. The affected lot number is 26025260, catalogue number ME2010.

What Products Are Being Recalled?

• Product: BD MaxPlus Connector Minibore Extension Set
• Brand: BD Switzerland Sarl
• Catalogue Number: ME2010
• Lot Number: 26025260
• Category: Health Products – Medical Devices – Dental
• Recall Class: Type I (most serious classification)

Why Was This Recall Issued?

BD has identified a mechanical issue with internal sterilization equipment at the manufacturing facility, which resulted in a potential under-dosing of the sterilization agent during product processing. This means the affected devices may not have been sterilized correctly and could pose a serious risk of infection if used in patient care.

A Type I recall is the most serious classification used by Health Canada, reserved for situations where there is a reasonable probability that the use of the product will cause serious adverse health consequences or death. The sterility failure in a medical device intended for healthcare use represents a significant patient safety concern.

Who Is Affected?

This recall is directed at the healthcare audience, including hospitals, clinics, dental offices, and other healthcare facilities that may have received or are currently using the BD MaxPlus Connector Minibore Extension Set from lot number 26025260. Patients who have received treatment involving this specific lot of devices may also be affected.

• Healthcare professionals using the BD MaxPlus Connector Minibore Extension Set
• Dental and medical facilities across Canada that received lot 26025260
• Patients who may have been treated with devices from this lot

What Should You Do?

Health Canada and BD Switzerland Sarl are urging all affected healthcare providers and facilities to take immediate action:

• Stop using any BD MaxPlus Connector Minibore Extension Set from lot number 26025260 immediately.
• Quarantine all remaining inventory from the affected lot and do not distribute or use the product.
• Contact the manufacturer, BD Switzerland Sarl, directly for additional information, return instructions, and guidance on replacement products.
• Report any adverse events or patient injuries potentially linked to the use of this product to Health Canada.
• Healthcare professionals should assess any patients who may have been treated using devices from the recalled lot and take appropriate clinical action.

Official Statement

According to Health Canada, BD Switzerland Sarl identified a mechanical issue with internal sterilization equipment resulting in potential under-dosing of product during processing, which may have resulted in product not being sterilized correctly. Health Canada classified this as a Type I recall, reflecting the severity of the potential health risk. The recall was published on June 19, 2026, and healthcare providers are strongly encouraged to act promptly. For further information, consumers and healthcare professionals can visit the Health Canada recalls and safety alerts portal or contact BD Switzerland Sarl directly at: Route De Crassier 17, Eysins, Switzerland, 1262.