BONE CURETTE-ANGLED 389.59

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2013-02-28 for BONE CURETTE-ANGLED 389.59 manufactured by Synthes Gmbh.

Event Text Entries

[3380719] It was reported that the instrument resin handles are leaching brown from the handle. This is 2 of 10 for the same event.
Patient Sequence No: 1, Text Type: D, B5


[10545981] Synthes is submitting this report as a result of remediation activities related to fda warning letter dated 02/2012. Device(s) listed in this report is (are) used for treatment, not diagnosis. Any additional information received regarding this event after filing this report shall be filed on a supplemental mdr. The sample was received in good condition. The instrument corresponds to drawings and processes according to manufacturing requirements. Discoloration was not found on the instrument. Measurable dimensions were found within tolerance. A review od the device history record did not show conditions that could have contributed to the reported event. This complaint is invalid from a manufacturing perspective.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number8030965-2013-10304
MDR Report Key3003358
Report Source06,07
Date Received2013-02-28
Date of Report2011-05-06
Date of Event2011-05-06
Date Mfgr Received2013-01-29
Device Manufacturer Date1999-01-01
Date Added to Maude2013-05-08
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 FDA0
Event Location0
Manufacturer ContactT. MCCARRON
Manufacturer Street1302 WRIGHTS LANE EAST
Manufacturer CityWEST CHESTER PA 19380
Manufacturer CountryUS
Manufacturer Postal19380
Manufacturer Phone8006207025
Manufacturer G1SYNTHES GMBH
Manufacturer StreetEIMATTSTRASSE 3
Manufacturer CityOBERDORF CH-4436
Manufacturer CountrySZ
Manufacturer Postal CodeCH-4436
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBONE CURETTE-ANGLED
Product CodeHTF
Date Received2013-02-28
Returned To Mfg2011-05-23
Catalog Number389.59
Lot NumberA7IA15
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSYNTHES GMBH
Manufacturer AddressOBERDORF SZ


Patients

Patient NumberTreatmentOutcomeDate
10 2013-02-28

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.