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Non-licensed inventory was sent to Canada via web shop orders starting in February of 2022. Recall start date: December 12, 2022

BVI has received a complaint from a customer that catalog # 376630 of the Beaver Edgehead Stiletto/Mvr knife 0.90 mm Straight (20g), a component of the Readpak kit (cat:584896, lots:6054175,6053035), was shipped with an open head. BVI is recalling the…

There is a potential malfunction with the side-port of the Triever 24. The side-port may potentially leak or dislodge during device preparation or during actual use. The side-port of the triever24 catheter is used in combination with a 60cc large bore…

Summit Medical received a customer complaint that Nasal Septal Button, 5cm, SP-78105 parts received from lot# 219349 were in unsealed pouched. The product was sterilized, but if this sterile barrier is not sealed, there is a possibility of product…

Cardinal Health has initiated a medical device correction for specific production lots of the Cardinal Health™ Jackson-Pratt™ channel drains. The recall is being issued due to various performance issues including lack of radiopacity in wound drains, dull…

The manufacturer of Statis SL handpieces has informed SciCan that the product may not function as expected if not properly maintained. When using the Statis handpieces, the lack of care or age-related wear and tear could result in the loosening parts…

Manufacturer initiated recall notifying users of variability of only the level 1 troponin I values included in the Mas CardioImmune XL controls (confirmed after 8 complaints). The level 1 control is included in lots of control kits CAI-XL 1, CAI-XL4…

In case the magnets of the Novastar TS and Novastar Plus are positioned near medical devices (implanted as well as not-implanted) and metallic implants the magnetic field might impact the implants or devices and cause serious injury. Recall start date…

The catheter repair adhesive used to attach the repair segment to the original catheter is hardened/coagulated (unusable). Recall start date: January 4, 2023

Defective hard drives were identified in the graphical user interface tablet of some devices. The defective component leads to tablet screen freeze and reboot occurrences, eventually rendering the transcranial doppler (TCD) ultrasound system inoperable…

This recall is being initiated to address a potential risk associated with use of the Visiusmatrix 4.0 devices. We have identified that the hardware equipment racks of the Visiusmatrix 4.0 devices at customer sites have not undergone all required aspects…

The recall is due to quality complaints from health care professionals that the gloves may not meet their intended use in a medical/surgical setting. The gloves easily tear and may result in potential harm, including contamination and disease…

Potentially compromised sterile barrier.  The conformity of the products was questioned by the German health authority due to packaging tests not adequately performed.  Single sterilized and transport conditioned according to ASTM d4169-22 was…

These pediatric nasal oxygen cannulas had sticky film when package was opened -  expired product or nearly expired product released placticizer film. Recall start date: December 05, 2022

Product was sold after device licence expired on March 31 2022. Recall start date: December 06, 2022