MAUDE Adverse Event Report: STRYKER ORTHOPAEDICS-MAHWAH 6.5MM LOW PROFILE HEX SCREW 30MM; PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

Catalog Number	7030-6530
Medical Device Problem Code	Malposition of Device (2616)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	04/29/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
It was noted that the device is not available for evaluation.A review of the device history records indicate that devices were manufactured and accepted into final stock with no reported discrepancies.There have been no other events for the lot referenced.If additional information is received, it will be provided in a supplemental report upon completion of the investigation.
Event or Problem Description
Surgeon notified rep that x-rays 1 week post op show a screw passed completely through the acetabular shell in the patient's right hip.It is not known at the time of report if the screw was implanted that way.The surgeon has not reported a plan to revise the patient at the time of report.Update 20 may, 2019: medical review confirmed the event and confirmed malposition of the screw as a root cause of the event.
Additional Manufacturer Narrative
An event regarding a screw passing completely through a shell involving a trident ii screw was reported.Medical review confirmed that the screw was malpositioned.Method & results -product evaluation and results: material analysis, visual, functional and dimensional inspections could not be performed as the device remained implanted -medical records received and evaluation: a review of the provided medical information by a clinical consultant indicated: malposition of a bone screw as used for supplemental screw fixation was caused by applying the screw in a rather oblique direction relative to the optimum.This caused the screw to cut through the sharp edge of the screw hole due to a local overload condition by point contact and thus become located behind the cup shell.It has lost the functionality but harm is not be expected, neither in short nor in long term due to its stable condition in the bone and the high biocompatibility of the materials involved.-product history review: a review of the device manufacturing records indicate that all devices accepted into final stock were free from discrepancies.-complaint history review: there have been no other similar events for the lot referenced.Conclusions: malposition of a bone screw as used for supplemental screw fixation was caused by applying the screw in a rather oblique direction relative to the optimum in a cup shell with malposition due to excessive anteversion with low inclination.This caused the screw head to cut through the sharp edge of the screw hole due to a local overload condition by point contact and thus become located behind the cup shell.It has lost the functionality but harm is not be expected, neither in short nor in long term due to its stable condition in the bone and the high biocompatibility of the materials involved.No further investigation for this event is required at this time.If devices and / or additional information become available to indicate further evaluation is warranted, this record will be reopened.
Event or Problem Description
Surgeon notified rep that x-rays 1 week post op show a screw passed completely through the acetabular shell in the patient's right hip.It is not known at the time of report if the screw was implanted that way.The surgeon has not reported a plan to revise the patient at the time of report.Update 20 may, 2019: medical review confirmed the event and confirmed malposition of the screw as a root cause of the event.

• Brand Name: 6.5MM LOW PROFILE HEX SCREW 30MM
• Common Device Name: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
• Manufacturer (Section D): STRYKER ORTHOPAEDICS-MAHWAH; 325 corporate drive; mahwah NJ 07430
• MDR Report Key: 8637436
• Report Number: 0002249697-2019-02088
• Device Sequence Number: 2211855
• Product Code: LPH
• UDI-Device Identifier: 07613327345063
• UDI-Public: 07613327345063
• Combination Product (Y/N): N
• Initial Reporter State: OR
• Initial Reporter Country: US
• PMA/510(K) Number: K171768
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: health professional,other
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 07/12/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Catalogue Number: 7030-6530
• Device Lot Number: 5T7A
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 04/29/2019
• Supplement Date Received by Manufacturer: 06/17/2019
• Initial Report FDA Received Date: 05/23/2019
• Supplement Report FDA Received Date: 07/12/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 46 YR