The Medical and Healthcare products Regulatory Authority have issued a device alert for the following items.
Wheeled and non-wheeled walking frames (all models) manufactured by Patterson Medical
(MDA/2013/060)
(MDA/2013/061)
Procedure packs containing BD Plastipack™ 50ml Luer Lok syringe manufactured by Kimal
(MDA/2013/065)
This Medical Device Alert has been issued as there is a risk of delay or interruption to treatment when affected syringes are used in power-driven syringe pumps. Kimal is recalling procedure packs containing BD syringes of the old design to avoid this risk.
PlastipakTM 50ml Luer Lok syringe – sterile manufactured by BD Medical
(MDA/2013/068)
(MDA/2013/069)
(MDA/2013/070)