WalkMed Infusion Recalls 2018 Triton Pole Mount Infusion Pumps Over Risk Of Pump Door Open Alarm Malfunction Which Could Lead To Over Infusion of Medication.
A Triton Pole Mount Infusion Pump recall has been issued by WalkMed Infusion LLC (“WalkMed Infusion”) recalling 2018 Triton Pole Mount Infusion Pumps reportedly because of the potential that the Triton Pole Mount Infusion Pump door open alarm might not function in certain door open positions which could lead to the infusion pump mechanism not to be engaged and a gravity feed flow condition to exist if the pump operator has not checked tube set for flow prior to starting the pump which could lead to over infusion of medications, according to a Food & Drug Administration (“FDA”) infusion pump recall news report.
The recalled Triton Pole Mount Infusion Pumps include infusion pumps with serial numbers 001 through 500 and serial numbers TR1401 through TR 2559 manufactured and sold before June 2010. Consumers who have the recalled Triton Pole Mount Infusion Pumps are reportedly being asked to return the pump to the manufacturer.
For more information on the WalkMed Infusion Triton Pole Mount Infusion Pump recall, call WalkMed Infusion at 1-303-420-9569 or visit the WalkMed Infusion website:
www.walkmed.net
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