MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2020-03-20 for BIPAP A40 1111169 manufactured by Philips Respironics Inc..
        [184260758]
The manufacturer received information alleging a patient became unresponsive and no alarm sounded while on a bipap a40. The patient was transferred to the icu and placed on mechanical ventilation and later expired. The device has yet to be returned to the manufacturer for evaluation. A follow up report will be filed when the manufacturer has completed the investigation.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2518422-2020-00661 | 
| MDR Report Key | 9859683 | 
| Report Source | FOREIGN,USER FACILITY | 
| Date Received | 2020-03-20 | 
| Date of Report | 2020-03-17 | 
| Date of Event | 2020-02-28 | 
| Date Mfgr Received | 2020-03-17 | 
| Device Manufacturer Date | 2015-06-16 | 
| Date Added to Maude | 2020-03-20 | 
| Event Key | 0 | 
| Report Source Code | Manufacturer report | 
| Manufacturer Link | Y | 
| Number of Patients in Event | 0 | 
| Adverse Event Flag | 3 | 
| Product Problem Flag | 3 | 
| Reprocessed and Reused Flag | 3 | 
| Health Professional | 3 | 
| Initial Report to FDA | 3 | 
| Report to FDA | 3 | 
| Event Location | 3 | 
| Manufacturer Contact | ADAM PRICE | 
| Manufacturer Street | 1001 MURRY RIDGE LANE | 
| Manufacturer City | MURRYSVILLE, PA | 
| Manufacturer Country | US | 
| Manufacturer G1 | PHILIPS RESPIRONICS INC. | 
| Manufacturer Street | 1001 MURRY RIDGE LANE | 
| Manufacturer City | MURRYSVILLE, PA | 
| Manufacturer Country | US | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | BIPAP A40 | 
| Generic Name | VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT, FACILITY USE | 
| Product Code | MNT | 
| Date Received | 2020-03-20 | 
| Model Number | 1111169 | 
| Catalog Number | 1111169 | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | N | 
| Device Eval'ed by Mfgr | R | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | PHILIPS RESPIRONICS INC. | 
| Manufacturer Address | 1001 MURRY RIDGE LANE MURRYSVILLE, PA US | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Death | 2020-03-20 |