CHEEK RETRACTOR, VARIABLE 62-00441

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2010-07-12 for CHEEK RETRACTOR, VARIABLE 62-00441 manufactured by Stryker Osteosynthesis Freiburg.

Event Text Entries

[14965393] During surgery, the tightening screw on the cheek retractor stripped.
Patient Sequence No: 1, Text Type: D, B5


[15515785] Device investigation in process, but not yet complete.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number8010177-2010-00260
MDR Report Key1760114
Report Source07
Date Received2010-07-12
Date of Report2010-06-14
Date of Event2010-06-14
Date Mfgr Received2010-06-14
Date Added to Maude2011-02-07
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 FDA0
Event Location0
Manufacturer ContactSHAWN KLOHA
Manufacturer Street750 TRADE CENTRE WAY STE 200
Manufacturer CityPORTAGE MI 49002
Manufacturer CountryUS
Manufacturer Postal49002
Manufacturer Phone2693245346
Manufacturer G1STRYKER OSTEOSYNTHESIS FREIBURG
Manufacturer StreetBOTZINGER STRASSE 41
Manufacturer CityFREIBURG D-79111
Manufacturer CountryGM
Manufacturer Postal CodeD-79111
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameCHEEK RETRACTOR, VARIABLE
Generic NameINSTRUMENT
Product CodeEIG
Date Received2010-07-12
Returned To Mfg2010-06-28
Model NumberNA
Catalog Number62-00441
Lot NumberZ5
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeNA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER OSTEOSYNTHESIS FREIBURG
Manufacturer AddressFREIBURG D-79111 GM D-79111


Patients

Patient NumberTreatmentOutcomeDate
10 2010-07-12

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