HIGH FLOW HEATED INSUFFLATOR TUBING (5BX) 0620030407

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2012-04-10 for HIGH FLOW HEATED INSUFFLATOR TUBING (5BX) 0620030407 manufactured by Stryker Endoscopy Puerto Rico.

Event Text Entries

[15858449] It was reported that a foreign substance was noticed on the polyethylene.
Patient Sequence No: 1, Text Type: D, B5


[15943035] Additional information will be provided once the investigation has been completed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2648666-2012-00121
MDR Report Key2540509
Report Source04
Date Received2012-04-10
Date of Report2012-03-15
Date of Event2012-03-16
Date Mfgr Received2012-03-15
Date Added to Maude2012-08-31
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 FDA0
Event Location0
Manufacturer ContactSUNNY OFFORJEBE
Manufacturer Street5900 OPTICAL CT.
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal95138
Manufacturer Phone4087542000
Manufacturer G1STRYKER ENDOSCOPY PUERTO RICO
Manufacturer StreetHWY. 3, KM. 130.2 LAS PALMAS INDUSTRIAL PARK
Manufacturer CityARROYO PR 00615
Manufacturer CountryUS
Manufacturer Postal Code00615
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHIGH FLOW HEATED INSUFFLATOR TUBING (5BX)
Generic NameINSUFFLATOR TUBING
Product CodeNKC
Date Received2012-04-10
Catalog Number0620030407
Lot Number11342FE2
OperatorOTHER
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ENDOSCOPY PUERTO RICO
Manufacturer AddressARROYO PR 00615 US 00615


Patients

Patient NumberTreatmentOutcomeDate
10 2012-04-10

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