MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US SOL SYS 10/13.5 R BOW; SOLUTION STEM IMPLANTS : HIP FEMORAL STEM

Model Number	1572-11-136
Medical Device Problem Code	Migration (4003)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	01/31/2022
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the patient had a periprosthetic of their competitor hemi hip prosthesis.The surgeon removed the indwelling hip and replaced it with a 10¿ bowed solution stem and a new hemi head/taper spacer on (b)(6) 2022.A few days after this surgery, the patient's hip dislocated.The surgeon determined that the stem rotated and needed to be replace with a larger diameter stem.This new procedure happened on (b)(6) 2022.The stem, head and taper spacer were all replaced.It was also indicated that there was loosening of the stem at the bone to implant interface.Doi: (b)(6) 2022, dor: (b)(6) 2022, affected side: right hip.
Additional Manufacturer Narrative
(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Additional Manufacturer Narrative
(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
It was reported that the patient had a periprosthetic of their competitor hemi hip prosthesis.The surgeon removed the indwelling hip and replaced it with a 10¿ bowed solution stem and a new hemi head/taper spacer on (b)(6) 2022.A few days after this surgery, the patient's hip dislocated.The surgeon determined that the stem rotated and needed to be replace with a larger diameter stem.This new procedure happened on (b)(6) 2022.The stem, head and taper spacer were all replaced.It was also indicated that there was loosening of the stem at the bone to implant interface.Doi: (b)(6) 2022, dor: (b)(6) 2022, affected side: right hip.
Additional 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: SOL SYS 10/13.5 R BOW
• Common Device Name: SOLUTION STEM IMPLANTS : HIP FEMORAL STEM
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• Manufacturer (Section G): DEPUY ORTHOPAEDICS, INC. 1818910; 700 orthopaedic dr.; warsaw IN 46581 0988
• Manufacturer Contact: kara ditty-bovard ; 700 orthopaedic dr.; warsaw, IN 46581-0988 ; 6107428552
• MDR Report Key: 13548474
• Report Number: 1818910-2022-02964
• Device Sequence Number: 5199857
• Product Code: LPH
• UDI-Device Identifier: 10603295061717
• UDI-Public: 10603295061717
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: K060581
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2022
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 02/17/2022

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
• Operator of Device: Health Professional
• Device Model Number: 1572-11-136
• Device Catalogue Number: 157211136
• Device Lot Number: JK0304
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/31/2022
• Supplement Date Received by Manufacturer: 03/15/2022
• Initial Report FDA Received Date: 02/17/2022
• Supplement Report FDA Received Date: 03/17/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 11/09/2021
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: MODULAR CATHCART BALL 44MM OD; SOL SYS 10/13.5 R BOW; TAPERED SPACER ARTICUL/EZE +0
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Female