PYXIS ANESTHESIA SYSTEM (PAS) PAS3500

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2018-10-26 for PYXIS ANESTHESIA SYSTEM (PAS) PAS3500 manufactured by Carefusion.

Event Text Entries

[126358632] (b)(4). Bd field service technician on site doing preventative maintenance work encountered sparking on the usb skateboard caused by a pinched cable. All affected parts were replaced and no further issues were identified.
Patient Sequence No: 1, Text Type: N, H10


[126358633] Bd employee encountered sparking when repairing the pas-3500 device. No harm was caused to a patient or the technician.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2016493-2018-00004
MDR Report Key8010142
Report SourceCOMPANY REPRESENTATIVE
Date Received2018-10-26
Date of Report2018-10-04
Date of Event2018-10-04
Date Mfgr Received2018-10-04
Device Manufacturer Date2009-01-01
Date Added to Maude2018-10-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. ALLISON SUAREZ
Manufacturer Street10020 PACIFIC MESA BLVD.
Manufacturer CitySAN DIEGO CA 92121
Manufacturer CountryUS
Manufacturer Postal92121
Manufacturer Phone8586174995
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePYXIS ANESTHESIA SYSTEM (PAS)
Generic NameAUTOMATED DISPENSING CABINET (ADC'S)
Product CodeBRY
Date Received2018-10-26
Model NumberPAS3500
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCAREFUSION
Manufacturer Address10020 PACIFIC MESA BLVD. SAN DIEGO CA 92121 US 92121


Patients

Patient NumberTreatmentOutcomeDate
10 2018-10-26

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