PRESTIGE ATRA GRASPER DBL-ACT 5MM 8360-10

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 2019-11-06 for PRESTIGE ATRA GRASPER DBL-ACT 5MM 8360-10 manufactured by Aesculap Inc.

Event Text Entries

[165408564] Manufacturing evaluation: investigation on-going. Additional information / investigation results will be provided in a supplemental report.
Patient Sequence No: 1, Text Type: N, H10


[165408565] It was reported that there was an issue with prestige graspers. The graspers were broken at the weld. The facility noted that this puts a strain on remaining instrument sets. There was no patient harm or intervention required. The incident occurred in surgery (to be confirmed). Additional information was not provided. Associated medwatches: 5 instruments reported separately.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2916714-2019-00113
MDR Report Key9286732
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-11-06
Date of Report2019-11-06
Date of Event2019-10-09
Date Mfgr Received2019-10-09
Date Added to Maude2019-11-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. LINDSAY CHROMIAK
Manufacturer Street3773 CORPORATE PARKWAY
Manufacturer CityCENTER VALLEY PA 18034
Manufacturer CountryUS
Manufacturer Postal18034
Manufacturer G1AESCULAP INC
Manufacturer Street3773 CORPORATE PARKWAY
Manufacturer CityCENTER VALLEY PA 18034
Manufacturer CountryUS
Manufacturer Postal Code18034
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePRESTIGE ATRA GRASPER DBL-ACT 5MM
Generic NameREUSABLE INSTRUMENTS
Product CodeNWV
Date Received2019-11-06
Model Number8360-10
Catalog Number8360-10
Lot NumberM48115
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP INC
Manufacturer Address3773 CORPORATE PARKWAY CENTER VALLEY PA 18034 US 18034


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-06

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