ROD TO ROD COUPLING HOFFMANN II COMPACT 5/5MM 49401010

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2016-09-14 for ROD TO ROD COUPLING HOFFMANN II COMPACT 5/5MM 49401010 manufactured by Stryker Gmbh.

Event Text Entries

[54675273] Once the investigation has been completed any additional information will be reported in a supplemental report.
Patient Sequence No: 1, Text Type: N, H10


[54675274] On (b)(6) 2016, the patient had surgery with a hoffmann2 compact. On (b)(6) 2016, the surgeon has tightened up more the rod coupling, the rod coupling broke.
Patient Sequence No: 1, Text Type: D, B5


[63644300] The reported incident that the rod to rod coupling hoffmann ii compact 5/5mm broke could be confirmed, since the returned device matched the reported event. Based on the investigation, the root cause was determined to be user related. The failure was caused by overtorqueing of the screw of the coupling. The device inspection revealed breakage of the screw is consistent with overtorqueing. Since this screw is the one that holds all of the pieces of the coupling together, it is natural that once it breaks, all of the components will fell off. It was reported that the instrument felt loosen and this is why the surgeon attempted to tighten again the screw, however upon this attempt, the strength used was so high that it caused the breakage of the screw. The looseness could not be confirmed since, not only the coupling was already broken, but also because not all of the coupling components were returned for investigation. Care should be taken not to overtighten the screw of the coupling as this may cause damages to the instrument, just like the present event. A review of the device history for the reported lot did not indicate any abnormalities. No corrective actions are required at this time. A review of the labeling did not indicate any abnormalities. No indications of material, manufacturing or design related problems were found during the investigation. If any further information is provided, the investigation report will be updated.
Patient Sequence No: 1, Text Type: N, H10


[63644301] On (b)(6) 2016, the patient had surgery with a hoffmann2 compact. On (b)(6) 2016, the surgeon has tightened up more the rod coupling, the rod coupling broke.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0008031020-2016-00448
MDR Report Key5949401
Report SourceHEALTH PROFESSIONAL
Date Received2016-09-14
Date of Report2016-12-29
Date of Event2016-08-16
Date Mfgr Received2016-12-01
Device Manufacturer Date2015-05-14
Date Added to Maude2016-09-14
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 FDA3
Event Location3
Manufacturer ContactMR. ANNA JUSINSKI
Manufacturer Street325 CORPORATE DRIVE
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal07430
Manufacturer Phone2018315000
Manufacturer G1STRYKER GMBH
Manufacturer StreetBOHNACKERWEG 1 POSTFACH
Manufacturer CitySELZACH 2545
Manufacturer CountryCH
Manufacturer Postal Code2545
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameROD TO ROD COUPLING HOFFMANN II COMPACT 5/5MM
Generic NameSMOOTH OR THREADED METALLIC BONE FIXATION FASTENER
Product CodeJEC
Date Received2016-09-14
Returned To Mfg2016-11-29
Catalog Number49401010
Lot NumberJ12745
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER GMBH
Manufacturer AddressBOHNACKERWEG 1 POSTFACH SELZACH 2545 CH 2545


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2016-09-14

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