The Medicines and Healthcare products Regulatory Agency (MHRA) of the United Kingdom posted a field safety notice concerning 22mm Flextube Transport Breathing Systems with non-rebreathing valve, manufactured by Intersurgical Limited. [REF numbers: 2070000, 2070001, 2073000, 2074000, 2075000 and 5020002; LOT numbers: from 31258704 to 31755743]
The manufacturer has voluntarily initiated a global recall of specific product codes and associated lots above of the 22mm Flextube Transport Breathing Systems with nonrebreathing valve. A fault has been identified in a non-rebreathing valve component in the affected products, and could result in an occlusion due to the valve sticking. If a ventilator with no self test facility is being used the fault may not be identified. The outcome for the patient will depend on a number of variables, including the degree of occlusion and how quickly the source of the problem is identified allowing remedial action to be taken.
According to the manufacturer, an internal assessment of product performance has confirmed that these devices can potentially raise serious risk to the patient. For this reason and to address any potential risk of harm, the affected products should not be used and should be destroyed.
The affected users are advised to stop the use of all affected devices immediately and ensure they are quarantined and destroyed. The manufacturer is working to resolve this situation and in the meantime they have an alternative replacement for the systems that do not have an adjustable PEEP valve or monitoring line (alternative Product code 2080004).
For details, please refer to the following link:
https://www.gov.uk/drug-device-alerts/field-safety-notice-14-to-18-august-2017
If you are in possession of the affected product, please contact your supplier for necessary actions.
Posted on 22 August 2017