PANETTI SUCTION INSTRUMENTS 30-1860

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-05 for PANETTI SUCTION INSTRUMENTS 30-1860 manufactured by Spiggle & Theis Medizintechnik Gmbh.

Event Text Entries

[129306399] The patient was taken to the operating room for revision of the right ossicular chain reconstruction, evaluation of re-current "choleastoma", and left sided removal of retained middle ear tube. The same peds panetti instrument set was used during this procedure, by the same surgeon. The surgeon was unable to establish suction through the instrument. The instrument was removed from the sterile field and flushed by the scrub tech on the back table. After flushing, debris appearing to be biological matter was expelled from the instrument. The sterile field was broken down, and the patient was re-prepped and re-draped. The instrument set was replaced. The vendor recommended cleaning the instruments using a 3 mach irrigation system and a high pressure water source. We do not own a 3 mach irrigation system, but was assured by the vendor that the in-house pure processing flexi-pump would provide adequate volume and pressure to flush the instruments efficiently and to decontaminate the instruments. We have subsequently been told the pure processing flexi-pump does not provide adequate volume and pressure to flush and decontaminate the instruments effectively. The pediatric operating room nursing staff also received in-service training of instrument use. This training did not include specific pre-cleaning instructions that, per the ifu, include using a wire to check inner lumen patency, rinsing instruments with a suitable cleaner or disinfectant, and storing instruments in a suitable cleaner or disinfectant if not processed within one hour after usage. The instruments were taken out of service to undergo further evaluation of the cleaning/decontamination process and determine patient exposure since the instruments sets were put in use. Manufacturer response for surgical instrument set, panetti endoscopic instrument set (per site reporter).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8132385
MDR Report Key8132385
Date Received2018-12-05
Date of Report2018-12-03
Date of Event2018-10-26
Report Date2018-12-03
Date Reported to FDA2018-12-03
Date Reported to Mfgr2018-12-05
Date Added to Maude2018-12-05
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePANETTI SUCTION INSTRUMENTS
Generic NameTUBE, EAR SUCTION
Product CodeJZF
Date Received2018-12-05
Model Number30-1860
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age6 MO
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerSPIGGLE & THEIS MEDIZINTECHNIK GMBH
Manufacturer AddressJEDMED 5416 JEDMED CT SAINT LOUIS MO 63129 US 63129


Patients

Patient NumberTreatmentOutcomeDate
10 2018-12-05

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