PNEUMATIC INFLATOR M00553200 5320

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2018-12-12 for PNEUMATIC INFLATOR M00553200 5320 manufactured by Boston Scientific Corporation.

Event Text Entries

[130050527] (b)(4). (b)(6). According to the complainant, the suspect device has been disposed and is not available for return. If any further relevant information is received, a supplemental mdr will be filed.
Patient Sequence No: 1, Text Type: N, H10


[130050528] It was reported to boston scientific corporation that a pneumatic inflator was used during an esophageal dilation procedure performed in the esophagus on (b)(6). 2018. According to the complainant, during the procedure, the gauge needle did not indicate any inflation. The procedure was completed with another pneumatic inflator. There were no patient complications reported as a result of this event. The patient's condition at the conclusion of the procedure was reported to be fine.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005099803-2018-61800
MDR Report Key8154662
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2018-12-12
Date of Report2019-02-14
Date of Event2018-11-20
Date Mfgr Received2019-01-16
Device Manufacturer Date2018-09-05
Date Added to Maude2018-12-12
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 ContactCAROLE MORLEY
Manufacturer Street300 BOSTON SCIENTIFIC WAY
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5086834015
Manufacturer G1NAVILYST MEDICAL
Manufacturer Street10 GLENS FALLS TECHNICAL PARK
Manufacturer CityGLENS FALLS NY 12801
Manufacturer CountryUS
Manufacturer Postal Code12801
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePNEUMATIC INFLATOR
Generic NameCATHETER, BALLOON TYPE
Product CodeGBA
Date Received2018-12-12
Model NumberM00553200
Catalog Number5320
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer Address300 BOSTON SCIENTIFIC WAY , MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
10 2018-12-12

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