MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2018-07-20 for PYXIS ANESTHESIA SYSTEM (PAS) PAS ES manufactured by Carefusion.
[114679123]
(b)(4). Field service technician on site found a burnt out light bulb. The bulb was replaced and no further issues were reported.
Patient Sequence No: 1, Text Type: N, H10
[114679124]
Customer reports visible smoke from the light bulb in the work lamp of the anesthesia device. No harm was caused to the patient or user.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2016493-2018-00002 |
MDR Report Key | 7707908 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2018-07-20 |
Date of Report | 2018-07-19 |
Date of Event | 2018-07-05 |
Date Mfgr Received | 2018-07-05 |
Device Manufacturer Date | 2018-03-01 |
Date Added to Maude | 2018-07-20 |
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 | MS. ALLISON SUAREZ |
Manufacturer Street | 10020 PACIFIC MESA BLVD. |
Manufacturer City | SAN DIEGO CA 92121 |
Manufacturer Country | US |
Manufacturer Postal | 92121 |
Manufacturer Phone | 8586174995 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PYXIS ANESTHESIA SYSTEM (PAS) |
Generic Name | AUTOMATED DISPENSING CABINET (ADC'S) |
Product Code | BRY |
Date Received | 2018-07-20 |
Model Number | PAS ES |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CAREFUSION |
Manufacturer Address | 10020 PACIFIC MESA BLVD. SAN DIEGO CA 92121 US 92121 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-07-20 |