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Displaying 1 - 15 of 409 items.
Affected lot may contain over-sized tablets.
RecallHealth product recall | 2023-11-27
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
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
GE Healthcare has become aware of the potential that incorrect torque has been applied to certain bolts of the Definium Tempo and Definium Tempo Pro products. This could result in a potential fall of elements of the overhead tube suspension (OTS) …
RecallHealth product recall | 2023-11-23
Inadequate product labelling at point of sale (end product distributed in bulk form)
RecallHealth product recall | 2023-11-14
Philips has identified an issue where a specific component failure in the gradient coil of the affected 1.5T MR systems listed in this letter may act as a heat source with a potential to produce smoke and/or fire. if the component failure occurs, the…
RecallHealth product recall | 2023-11-06
BD is issuing a notification to inform customers that Cardinal Health branded Monoject™ syringes have not been validated for use with the BD Alaris™ infusion devices. BD has validated Covidien branded Monoject™ syringes for use with the BD Alaris™…
RecallHealth product recall | 2023-10-30
CHS initiated this recall after receiving a recall letter from Baxter which stated that: "This action is being taken as a precautionary measure as there may be a potential for leaking or dislodged membrane ports on the solution bags during the spiking…
RecallHealth product recall | 2023-10-30
BD is issuing a notification to inform customers that Cardinal Health branded Monoject™ syringes have not been validated for use with the BD Alaris™ infusion devices. BD has validated Covidien branded Monoject™ syringes for use with the BD Alaris™…
RecallHealth product recall | 2023-10-30
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