It was reported the patient increased her remodulin and felt great, but when she changed her disposable, she became fatigued and had increased chest pressure.When she changed the disposable and pump, she felt a lot better.
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Other, other text: a1 updated, b3: unknown.D4: catalog number, udi number, and serial number is unknown; g5: 510k is unknown; h4: device manufacture date is unknown.D1, d3: unknown.No product was returned.We are unable to confirm the reported complaint.If the product is returned, the manufacturer will reopen this complaint for further investigation.The most probable cause for a delivery inaccuracy is the pump's expulsor; however, this cannot be confirmed as no product was returned for investigation.No serial number was provided; therefore, a device history record (dhr) review could not be conducted.
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