MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US SUMMIT BASIC PRESS FIT SZ 6; SUMMIT HIP STEM : HIP FEMORAL STEM

Model Number 1570-05-120

Device Problem Osseointegration Problem (3003)

Patient Problems Bone Fracture(s) (1870); Inadequate Osseointegration (2646)

Event Date 12/08/2020

Event Type  Injury  

Manufacturer Narrative

Product complaint #: (b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

Event Description

The patient was revised bipolar hip construct to address periprosthetic femoral fracture and loosening of the stem at the bone to implant interface.Summit basic stem bipolar construct was removed and replaced with a reclaim stem and bipolar.Doi: (b)(6) 2020, dor: (b)(6) 2020, left hip.

Manufacturer Narrative

Product complaint # (b)(4).Investigation summary : no device associated with this report was received for examination.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed, and the investigation will be re-opened as necessary.Device history lot : the product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).A manufacturing records evaluation (mre) was not performed.

• Brand Name: SUMMIT BASIC PRESS FIT SZ 6
• Type of Device: SUMMIT HIP STEM : HIP FEMORAL STEM
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 11057121
• MDR Text Key: 223185788
• Report Number: 1818910-2020-27522
• Device Sequence Number: 1
• Product Code: LWJ
• UDI-Device Identifier: 10603295059721
• UDI-Public: 10603295059721
• Combination Product (y/n): N
• PMA/PMN Number: K030122
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,health
• Type of Report: Initial,Followup
• Report Date: 12/08/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 1570-05-120
• Device Catalogue Number: 157005120
• Device Lot Number: D17010503
• Was Device Available for Evaluation?: No
• Initial Date Manufacturer Received: 12/08/2020
• Initial Date FDA Received: 12/22/2020
• Supplement Dates Manufacturer Received: 01/21/2021
• Supplement Dates FDA Received: 01/22/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Treatment: ARTICUL/EZE BALL 28 +1.5 GR; SELF CENT HIP 44X28 GRY; ARTICUL/EZE BALL 28 +1.5 GR; SELF CENT HIP 44X28 GRY
• Patient Outcome(s): Required Intervention
• Patient Age: 82 YR