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Displaying 1 - 15 of 4189 items.
Affected lot may contain over-sized tablets.
RecallHealth product recall | 2023-11-27
During an update of data used in a library shipped with Exoplan or made available on the download portal of Exocad, it was found that the use of a specific combination of an implant, sleeve and surgical drill can result in a hole being drilled 1 mm…
RecallHealth product recall | 2023-11-27
Olympus has identified a total of 1003 complaints, including 372 adverse events (since September 2020 to August 2023) related to pink or green coloration of the image, including cases with reported delays of treatments and/or prolonged surgery. Olympus…
RecallHealth product recall | 2023-11-27
Through an internal investigation, it was identified that there is a defect in the outer packaging of the cranial access kits. This defect can cause the packaging to split without any additional forces outside of regular manufacturing and sterilization/…
RecallHealth product recall | 2023-11-27
Ortho Cinical Diagnostics (quidelortho) has determined that some lots from coating 3598 of Vitros Eco2 Slides include carts which may contain consecutive slides that may not function as intended. These affected Vitros Eco2 slides (potentially…
RecallHealth product recall | 2023-11-24
Solution bags may be leaking in affected lots.
RecallHealth product recall | 2023-11-24
Solution bags may be leaking in affected lots.
RecallHealth product recall | 2023-11-24
Solution bags may be leaking in affected lots.
RecallHealth product recall | 2023-11-24
Solution bags may be leaking in affected lots.
RecallHealth product recall | 2023-11-24
Philips has identified a potential safety issue with the Philips Allura and Azurion product families having monoplane fixed ceiling mounted systems. The ceiling mounted l-arm contains a rotation cover that may potentially be susceptible to falling if a…
RecallHealth product recall | 2023-11-24
XPRSTREPA-CE-10 kits packaged with defective pipettes may cause failure to dispense an adequate volume of the patient sample to the test cartridge. If there is inadequate volume of patient sample being tested, the customer may receive an 'invalid' or 'no…
RecallHealth product recall | 2023-11-24
The outer jacket of the tank hose assembly does not have the specified pin perforations due to supplier oversight. Gas could get trapped on non-pin perforated hoses under the outer jacketing of the hose, forming a distension.
Recall start date:…
RecallHealth product recall | 2023-11-24
Smiths Medical identified legacy software anomalies which may occur in the Medfusion 3500 syringe infusion pumps. the legacy software anomalies were identified during a historical review of the risk evaluations conducted during the software development…
RecallHealth product recall | 2023-11-23
Smiths Medical identified legacy software anomalies which may occur in the Medfusion 4000 syringe infusion pumps. The legacy software anomalies were identified during a historical review of the risk evaluations conducted during the software development…
RecallHealth product recall | 2023-11-23
In rare cases, an ECG failure affecting impedance measurement via defibrillation electrodes has led to the Defigard Touch-7 falsely reports an electrode fault, resulting in inoperative defibrillation.
Recall start date: November 14, 2023
RecallHealth product recall | 2023-11-23