CYTOSPONGE CELL COLLECTION DEVICE CYTO-KITR

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,study report with the FDA on 2015-11-18 for CYTOSPONGE CELL COLLECTION DEVICE CYTO-KITR manufactured by Medtronic.

Event Text Entries

[31525454] (b)(4). To date the incident sample has not been received for evaluation. If the sample is received or if additional information pertinent to the incident is obtained a follow-up report will be submitted. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[31525455] It was reported that patient was experiencing severe pain for 3-4 days following cytosponge procedure. Patient reported difficulty eating solid food. Patient proceeded to take heartburn medication to relieve the pain. Patient reported black stool for 3 days. Pain resolved.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004904811-2015-00030
MDR Report Key5233549
Report SourceHEALTH PROFESSIONAL,STUDY
Date Received2015-11-18
Date of Report2015-10-20
Date of Event2015-10-20
Date Mfgr Received2015-10-20
Date Added to Maude2015-11-18
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 ContactSHARON MURPHY
Manufacturer Street540 OAKMEAD PARKWAY
Manufacturer CitySUNNYVALE CA 94085
Manufacturer CountryUS
Manufacturer Postal94085
Manufacturer Phone2034925267
Manufacturer G1MEDTRONIC
Manufacturer Street540 OAKMEAD PARKWAY
Manufacturer CitySUNNYVALE CA 94085
Manufacturer CountryUS
Manufacturer Postal Code94085
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCYTOSPONGE CELL COLLECTION DEVICE
Generic NameESOPHAGOSCOPE
Product CodeEOX
Date Received2015-11-18
Model NumberCYTO-KITR
Catalog NumberCYTO-KITR
Lot NumberF2500042X
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC
Manufacturer Address540 OAKMEAD PARKWAY SUNNYVALE CA 94085 US 94085


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-11-18

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