The device was returned for evaluation.The device evaluation found the fuse was blown, blood was found in power supply, and there was a burning smell, however, there was no evidence of burning or carbonization within the device.The following parts were replaced due to blood spill; power supply, dc wire harness, ac line filter, centrifuge, cables and top deck distribution board.All the parts in the chassis had to be removed due to blood and the drain tube housing being clogged by clotted blood.The device was cleaned, repaired and upgraded to the current fluid ingress remediation to mitigate damage caused if fluid enters into the body of the orthopat device.Haemonetics (b)(4).
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