3.5 MM PEEK TWINLOOP FLEX ONE STRAND 2 FORCE FIBER 3910-405-638

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 2012-06-05 for 3.5 MM PEEK TWINLOOP FLEX ONE STRAND 2 FORCE FIBER 3910-405-638 manufactured by Stryker Endoscopy Puerto Rico.

Event Text Entries

[2644125] It was reported that during a shoulder arthroscopy procedure, after the surgeon implanted the anchor, the thread broke and separated from the anchor unit. The account reports that this has occurred before. The procedure was completed successfully with another item.
Patient Sequence No: 1, Text Type: D, B5


[9884261] A quantity of three units, from the same lot number, were implicated in this event. A separate report will be issued for each individual unit. Add'l info will be provided once the investigation has been completed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2648666-2012-00192
MDR Report Key2607940
Report Source07
Date Received2012-06-05
Date of Report2012-05-11
Date of Event2012-05-07
Date Mfgr Received2012-05-11
Date Added to Maude2012-10-02
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 ContactTOM SHAFER
Manufacturer Street5900 OPTICAL COURT
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal95138
Manufacturer Phone4087542000
Manufacturer G1STRYKER ENDOSCOPY PUERTO RICO
Manufacturer StreetHWY. 3, KM. 130.2 LAS PALMAS IND. PARK
Manufacturer CityARROYO PR 00615
Manufacturer CountryUS
Manufacturer Postal Code00615
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name3.5 MM PEEK TWINLOOP FLEX ONE STRAND 2 FORCE FIBER
Generic NameSHOULDER FIXATION ANCHOR
Product CodeNOV
Date Received2012-06-05
Catalog Number3910-405-638
Lot Number11276AE2
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ENDOSCOPY PUERTO RICO
Manufacturer AddressARROYO PR 00615 US 00615


Patients

Patient NumberTreatmentOutcomeDate
10 2012-06-05

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