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Displaying 1 - 9 of 9 items.
Olympus is providing updated warning and recommendations after being aware of patients suffering complications from over insufflation including arrythmias, gas embolism, and death during surgical procedures.
Recall start date: October 13, 2023
RecallHealth product recall | 2023-10-30
The manufacturer received three reports that during processing and preparation of the room setup the monitor suspension disconnected from the height adjustable arm construction. This affects all lots of the lightweight spring arm (part numbers 42A-43L,…
RecallHealth product recall | 2023-10-18
The pumps have the potential for the upstream occlusion sensor to cease proper function due to the build-up of electrostatic charge during operation triggering false downstream and upstream occlusion alarms.
Recall Start Date: August 28, 2023
RecallHealth product recall | 2023-09-07
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…
RecallHealth product recall | 2023-08-24
Medtronic was made aware of a supplier calibration issue during the contract sterilization process that may lead to unsterile product.
Recall start date: March 1, 2023
RecallHealth product recall | 2023-03-17
Specific lots have the potential for a broken sled vane component. A broken sled vane may cause the reload to misfire leading to non-functional staple line closure, transecting tissue without forming staples, and tissue hang-up. These conditions may…
RecallHealth product recall | 2023-02-08
Intuitive has become aware of the potential for unexpected motion caused due to partial disengagement of the instrument from the system while using the da vinci s/si and x/xi Endowrist clip applier instruments. Intuitive has received several complaints…
RecallHealth product recall | 2022-07-11
During verification testing, a non-conformance was detected. Failure mode was uncontrolled leakage of glue from the distal tip of the Fix8 open (FX002) device.
Recall start date: Feb 3, 2022
RecallHealth product recall | 2022-02-14
Hillrom received four (4) complaints between 29-Sep-2020 and 09-Apr-2021 of the Slingbar 450 becoming detached from the upper bracket of the Slingbar attachment on Liko M230 Mobile Lifts. The Slingbar is attached to the lifting arm through two brackets.…
RecallHealth product recall | 2022-01-24