MEDITECH 50-100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1993-04-27 for MEDITECH 50-100 manufactured by Boston Scientific Corporation.

Event Text Entries

[3071] On 1 mar 93 patient began to run an elevated temperature. Patient was sent to radiology for exam on 3 mar 93. Exam revealed part of insertion system still in patient. On 10 mar 93 patient was taken to cath lab & piece was removed. Patient suffered no injury from incident. Piece removed was distal portion of stylet rod (6 cm) which resides in carrier capsule. Investigation begun 11 mar 93. Investigation and review concluded 31 mar 93. It was determined that there was noted no difficulty inserting filter. Review of medical/surgical reports confirm routine insertion. Also interviewed staff. Conclusion of investigation was that style was most probably broken inside carrier. Was kept in place by filter during insertion, upon withdrawal stylet worked loose from carrier and was left behindinvalid data - regarding single use labeling of device. Patient medical status prior to event: fair condition. There was not multiple patient involvement. Invalid data - on device service/maintenance. No data - regarding date last serviced. Service provided by: invalid data. Invalid data - service records availability. Invalid data - regarding whether event presents imminent hazard. Device used as labeled/intended. Device was evaluated after the event. Method of evaluation: actual device involved in incident was evaluated, visual examination. Results of evaluation: other. Conclusion: device failure directly caused event. Certainty of device as cause of or contributor to event: yes. Corrective actions: none or unknown. The device was destroyed/disposed of.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number5192
MDR Report Key5192
Date Received1993-04-27
Date of Report1993-03-31
Date of Event1993-02-22
Date Facility Aware1993-03-09
Report Date1993-03-31
Date Reported to Mfgr1993-03-09
Date Added to Maude1993-06-30
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameMEDITECH
Generic NameVENA CAVA FILTER
Product CodeLWT
Date Received1993-04-27
Model Number50-100
Lot Number38888
Device Expiration Date1993-11-01
OperatorOTHER HEALTH CARE PROFESSIONAL
Device AvailabilityN
Implant FlagY
Device Sequence No1
Device Event Key4893
ManufacturerBOSTON SCIENTIFIC CORPORATION


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1993-04-27

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