Alerts

Recall due to potential for user injury as a result of device breakage.

Recall for product correction due to potential for user injury.

Hazard alert due to potential for post-operative infection.

Recall - risk of plastic fragments breaking from bottle and being ingested

Recall - risk of plastic fragments breaking from bottle and being ingested

Update - recall - additional batch affected

Recall - potential for particle contamination

Hazard alert due to higher-than-expected revision rates.

Recall – potential for contamination with latex

Hazard alert update due to additional issue that can result in an unintended device software reset.

Hazard alert due to potential for component failure due to metal fracture.

Hazard alert due to the risk of implant breakage that could cause adverse events and require additional surgery.

Update - recall - additional batches affected

Recall - risk of plastic fragments breaking from bottle and being ingested

Hazard alert due to warnings regarding potential adverse events.

Recall for product correction due to potential for interruption of medicine delivery and/or infection due to needle breaking during use.

Recall for product correction due to potential for interruption of insulin delivery and/or infection due to needle breaking during use.

Multiple devices which use auto servo ventilation/Adaptive Servo-Ventilation (ASV) therapy have been subject to recall actions.

Recall for product correction due to increased risk of death for patients with symptomatic chronic heart failure.

Recall for product correction due to additional affected devices.

Recall as pumps will cease operation on 1 January 2016.

Recall - risk of adverse events due to unacceptably high level of arsenic

Hazard alert due to multiple potential safety issues.

Recall for product correction due to fire risk from faulty component.

Recall for product correction due to fire risk from faulty component.