WARMER DRAPE ORS-300

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 2018-02-06 for WARMER DRAPE ORS-300 manufactured by Microtek Dominicana, S.a..

Event Text Entries

[99792857] The dhr was reviewed and it was noticed that this lot had 4800 pieces that were manufactured from 7/26/2017 to 7/27/2017. No defects were reported during quality inspections. Based on the dhr, this does not appear to be the result of a personnel, process or material issue. At the time of this report, the device had not been returned for evaluation. As no device was available for evaluation, the root cause of this complaint cannot be confirmed. If additional information becomes available, a follow up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[99792858] The customer is reporting that they found a hole in a drape. No injury or treatment was reported for the incident.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8043817-2018-00004
MDR Report Key7246201
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2018-02-06
Date of Report2018-01-31
Date Mfgr Received2018-01-31
Date Added to Maude2018-02-06
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 ContactMRS JENNIFER MRKVICKA
Manufacturer Street1 ECOLAB PLACE
Manufacturer CityST. PAUL MN 55102
Manufacturer CountryUS
Manufacturer Postal55102
Manufacturer Phone6512502237
Manufacturer G1MICROTEK DOMINICANA
Manufacturer StreetZONA FRANCA NO. 2
Manufacturer CityLA ROMANA,
Manufacturer CountryDR
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameWARMER DRAPE
Generic NameFLUID WARMING AND SLUSH DRAPES
Product CodeLHC
Date Received2018-02-06
Model NumberORS-300
Lot NumberD172079
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMICROTEK DOMINICANA, S.A.
Manufacturer AddressZONA FRANCA NO. 2 LA ROMANA, DR


Patients

Patient NumberTreatmentOutcomeDate
10 2018-02-06

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