Sign-up to one of our many Group Actions today - use our quick and easy form to start your claim for compensation.
There is a reported risk with the use of non-recommended syringes in Alaris syringe pumps, manufactured by CareFusion.
The non-recommended syringes are reported to have a broken spring in the plunger which may cause unintended bolus (usually chewed up mass in the mouth) of medication.
The problem wasn’t identified by the medical technology manufacturer, and was instead brought to the attention of the Medicines and Healthcare products Regulatory Agency (MHRA) who then issued a medical device alert on 22 December 2016.
The medical device alert notes the following action points:
All staff who use these devices should undertake these actions no later than 7 February 2017. To minimise the risk of built up bolus of medication, it’s advisable that non-recommended syringes with a pump that has a broken spring shouldn’t be used with the syringe driver plunger.
CareFusion notes that there hasn’t been an increased risk of this problem when recommended syringes are used with the pumps.
The content of this post/page was considered accurate at the time of the original posting and/or at the time of any posted revision. The content of this page may, therefore, be out of date. The information contained within this page does not constitute legal advice. Any reliance you place on the information contained within this page is done so at your own risk.