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Other Medical Devices

🏥 Medical Devices 15,203 recalls

Additional Caution statements in IFU: (1) Due to complaints where the loop wire at the distal end of the HF resection electrode broke after getting in contact with metal objects, such as other endoscopic equipment, implants or stents. As a result, fragments can fall inside the patient and must be retrieved. (2) The second Caution refers to the risk of sparkover when getting in contact with metal parts as this can cause uncontrolled heating of the HF-resection electrode and may result in damage and breakage to the HF-resection electrode tip

Jun 8, 2023 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

Jun 28, 2023 Other Medical Devices Nationwide View Details →

Infinity FMS Pak

Alcon Research

Class I - Dangerous

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

Jun 28, 2023 Other Medical Devices Nationwide View Details →

Alcon Custom Pak

Alcon Research

Class I - Dangerous

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

Jun 28, 2023 Other Medical Devices Nationwide View Details →

If blood glucose monitoring system users attempt to start a new sensor, when the old sensor wasn't used for the full 14-day wear time, then the reader may display "Incompatible Sensor" message. If users don't have the previous sensor, or FreeStyle Libre 2 app, or the sensor's full wear time hasn't ended, users may be unable to start a new sensor, which could result in no or delayed glucose results

Jul 12, 2023 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

Jun 28, 2023 Other Medical Devices Nationwide View Details →

Carryover from the Direct LDL-cholesterol assay on the Rx instruments may result in a negative bias, up to -11%, in quality control and patient samples, in urea assays results if the urea assay is run immediately after the Direct LDL-cholesterol assay. This may lead to a delay in reporting results or in falsely decreased urea test results.

Jun 13, 2023 Other Medical Devices Nationwide View Details →

During installation of the SmokeDetector Interlock, a connecting cable, between the SmokeDetector Interlock and the host PC, may not have been properly installed. This connection is used for service diagnostics and does not impact the functionality of the system and/or the SmokeDetector Interlock system.

Jun 12, 2023 Other Medical Devices Nationwide View Details →

During installation of the SmokeDetector Interlock, a connecting cable, between the SmokeDetector Interlock and the host PC, may not have been properly installed. This connection is used for service diagnostics and does not impact the functionality of the system and/or the SmokeDetector Interlock system.

Jun 12, 2023 Other Medical Devices Nationwide View Details →

Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the LF-V and LF-P are no longer compatible endoscopes for reprocessing in the OERs. The addendum highlights the following changes: 1. Removal of LF-V and LF-P as compatible with the OER 2. Change conditions for ETO gas sterilization from 12% EtO to 100% EtO 3. Removing the reusable cleaning brush for the manual cleaning. Single Use brushes remain compatible

May 26, 2023 Other Medical Devices Nationwide View Details →

The C-arm, used to set the position and angle of the x-ray exposure field, may not function due to the tableside console PWB, which needs replacement. There may be a delay in the procedure, but procedures can continue using the operators console, the switches on the back of the column, switches on the side of the flat panel detector, and the emergency stop will continue to function normally.

Jun 22, 2023 Other Medical Devices Nationwide View Details →

HoverMatt, 39" W x 78" L, REF: HM39SPU-B

Stryker Sustainability Solutions

Class I - Dangerous

39-inche-wide inflatable air transfer mattress packages contain 34-Inch-wide mattresses, so there may be a decreased surface area available to distribute the patient's weight across, which may increase the effort exerted by staff for a lateral patient transfer, and there may be increased friction and shearing forces when the patient is moved resulting in skin tear injury.

Jun 21, 2023 Other Medical Devices View Details →

Thread form issue of the locking holes in that the locking screws would not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock.

Jun 27, 2023 Other Medical Devices View Details →