989803182301

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-08 for 989803182301 manufactured by Philips Medical Systems.

Event Text Entries

[144671768] Serial number not provided. A follow-up report will be submitted once the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10


[144671769] The customer stated that the blood pressure cuff "popped" or " exploded". The bp cuff was noted to have a 2cm hole near the crease side (not the seam side) where it popped. Near to where the arrow and label " arteria" are located. There was no reported patient incident injury.
Patient Sequence No: 1, Text Type: D, B5


[144688000] .
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1218950-2019-03305
MDR Report Key8590437
Date Received2019-05-08
Date of Report2019-04-16
Date Mfgr Received2019-04-16
Date Added to Maude2019-05-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. ROBERT CORNING
Manufacturer Street3000 MINUTEMAN ROAD
Manufacturer CityANDOVER MA 01810
Manufacturer CountryUS
Manufacturer Postal01810
Manufacturer Phone9786871501
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameNA
Generic NameSINGLE CARE CUFF, ADULT
Product CodeDXQ
Date Received2019-05-08
Model Number989803182301
Catalog Number989803182301
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerPHILIPS MEDICAL SYSTEMS
Manufacturer Address3000 MINUTEMAN ROAD ANDOVER MA 01810 US 01810


Patients

Patient NumberTreatmentOutcomeDate
10 2019-05-08

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.