MAUDE Adverse Event Report: DEPUY INTERNATIONAL LTD - 8010379 S-ROM*SLEEVE PRX ZTT, 22F-XXL; S-ROM HIP SYSTEM : HIP FEMORAL SLEEVE

Catalog Number 550550

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Foreign Body Reaction (1868); Hypersensitivity/Allergic reaction (1907); Inflammation (1932); Pain (1994); Osteolysis (2377); Swelling/ Edema (4577)

Event Date 04/28/2022

Event Type  Injury  

Manufacturer Narrative

Product complaint # (b)(4).This report is being submitted pursuant to the provisions of 21 cfr, part 803 (and/or part 4, as applicable).This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by depuy synthes, or its employees that the report constitutes an admission that the product, depuy synthes, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.

Event Description

The patient was revised due to pain, pseudotumor, and metallosis of the left hip secondary to failed metal-on-metal bearing surfaces.It was also noted there was atleast 50% loss of bone around the entire acetabular component.The cup was well fixed and further attempts to remove the cup with palpitation revealed to be quite solid to the remaining bone.The cup was not removed.The patient's greater trochanter and entire proximal femur had disappeared secondary to osteolysis.Ct scan reported of large periprosthetic fluid collection.Doi: (b)(6) 2007 dor: (b)(6) 2022 (metal liner and head) left hip.

Manufacturer Narrative

Product complaint # (b)(4).Investigation summary - no device associated with this report was received for examination.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 records evaluation (mre) was not performed.As part of our company quality system process, all devices are manufactured, inspected, and distributed to approved specifications.Additional complaint information monitoring for potential safety signals will be conducted through complaint trending as part of the post-market surveillance.If additional information is made available, the investigation will be updated as applicable.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.H10 additional narrative: added: b5, b7.

Event Description

Medical records received.Doi: (b)(6) 2007: male patient with a history of left hip femoral fracture, left hip competitor orif, left hip competitor tha, acetabular and femoral osteolysis, and chronic sepsis infection received a depuy mom revision tha as stage 2 treatment of infection.The acetabular cup was secured with a dome screw and the acetabular osteolysis required bone grafting.The previous femoral fracture site was partially healed and required a larger bone cut and the use of an s-rom stem and sleeve.The surgeons noted there was some shortening of the left leg because of the preexisting fracture caused by an mva.The procedure was completed without complications.Ct scan and preoperative testing (b)(6) 2024: a male patient is referred for revision surgery after failed attempts at treating chronic left hip pain.Preoperative aspiration does not detect elevated serum or synovial heavy metal ions but does detect elevated inflammatory markers.Ct scans identify a large pseudotumor as well as extensive acetabular and femoral osteolysis.These were preexisting events and are part of the treatment of revision captured on (b)(4).

• Type of Device: S-ROM HIP SYSTEM : HIP FEMORAL SLEEVE
• Manufacturer (Section D): DEPUY INTERNATIONAL LTD - 8010379; st. anthony's road; leeds LS11 8DT; UK LS11 8DT
• Manufacturer (Section G): JTE WARSAW MFG SITE; 700 orthopaedic drive; warsaw IN
• Manufacturer Contact: kate karberg ; 700 orthopaedic dr.; warsaw, IN 46581-0988 ; 3035526892
• MDR Report Key: 19051321
• MDR Text Key: 339491342
• Report Number: 1818910-2024-07660
• Device Sequence Number: 1
• Product Code: LPH
• UDI-Device Identifier: 10603295175421
• UDI-Public: 10603295175421
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: P070026
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 04/05/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 04/05/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 08/07/2011
• Device Catalogue Number: 550550
• Device Lot Number: 2185926
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 04/11/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 08/08/2006
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: 11/13 S-ROM 44MM M SPEC+9; PINN CAN BONE SCREW 6.5MMX15MM; PINN CAN BONE SCREW 6.5MMX15MM; PINN CAN BONE SCREW 6.5MMX15MM; PINNACLE MTL INS NEUT44IDX64OD; PINNACLE REV ACET CUP 70MM; SROM*STM LG 36+8L 22X17X230L
• Patient Outcome(s): Required Intervention
• Patient Age: 59 YR
• Patient Sex: Male