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Olympus found that certain lots of the CV-190 do not start up properly and as a result, the image from the endoscope is not displayed when the operations listed below are performed because parts that deviated from the specification were assembled into…

The shaft and tip component of the Universal Joint Screwdriver was manufactured with the incorrect raw stainless steel material. Recall start date: September 1, 2023

Siemens Healthcare will be informing customers about potential dot- or line-shaped artifacts caused by the presence of lubricating grease within the headband of the over-ear headphones listed below when used during head examinations with the Magnetom MRI…

Immucor, Inc. has indicated that this medical device recall is to communicate that some vials of Capture-CMV indicator red cells may contain particulates. The particulates are associated with fungal growth in the vials. Recall Start Date: August 24,…

Arjo has observed an increasing complaint trend on the following failure modes occurring on Arjo medical beds assembled with the Indigo modules: unanticipated device self-acceleration while being operated by a caregiver, unexpected movement without any…

Some Phoroptor VRx devices may have an assembly defect that causes the device to detach from the bracket that connects it to an ophthalmic stand. A device that detaches from a stand can fall on to a patient or operator causing an injury. The defect was…

The Equipro High Frequency Portable EI-113P is non-compliant (not licensed for sale in Canada) as a Class II medical device under Canadian law. Further distribution or use of the remaining product must stop immediately. Please notify any customers to…

Stryker has discovered the potential for the Triathlon Fixation Peg to be missing the hex hole feature preventing the peg from assembling with the slip torque handle. Recall start date: August 21, 2023

Medline recalls sterile 4.5" iris scissors (dynj04049); tip protector may detach, risking unseen punctures in the sterile barrier. Recall start date: August 11, 2023

Cardinal Health Canada has been notified of an urgent product recall initiated by Ecolab for the equipment drapes, table cover, and surgical room turnover (SRT) kits. Ecolab as Microtek has received odor complaints on certain lots. The odor has been…

The calibration of the force sensor used to detect occlusions may shift over time. If the force sensor calibration shift is large enough, the pump will display a system failure alarm (including force sensor BGND test, force sensor bridge test, or force…

The packaging containing a pair of sterilized surgical gloves is not sufficiently sealed potentially compromising the sterility assurance of the product. Recall start date: August 3, 2023

A single lot (74M2001125) of the one-way valve (part #50412 (pack of 5)) utilized with the Inomax dsir plus is being recalled. The one-way valve is used to prevent reverse flow into the Inomax dsir injector module from high frequency ventilators and…

Ethicon received seven complaints for one lot of undyed PDS™ II sutures regarding low tensile strength. Internal testing on returned product from this lot confirmed that some PDS™ II sutures from this lot did not meet Ethicon's tensile strength…

Abbott has received complaints from patients who are unable to exit MRI mode, as their patient controller has lost the ability to connect or communicate with their IPG while in MRI mode. Abbott sent a customer communication on 2023-07-21 to remind health…