DJO SURGICAL 425-97-013Recalls & reported problems
Encore Medical, L.P. · TAPERFILL HIP STEM, LATERAL OFFSET, SIZE 13 · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 15
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00888912078719), received between May 13, 2019 and Feb 16, 2026 — classified as 15 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem8
- Appropriate Device Problem Term/Code Not Available2
- Device Dislodged or Dislocated2
- Fracture2
- Device Slipped1
- Loose or Intermittent Connection1
Patient problems
- Bone Fracture(s)4
- Fall4
- Joint Laxity2
- Pain2
- Failure of Implant1
- Injury1
- Insufficient Information1
- Limb Fracture1
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
InjuryFeb 16, 2026Fracture
InjuryNov 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMay 6, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryApr 3, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO PATIENT FELL A FEW WEEKS POST OPERATIVELY AND HAD A PERIPROSTHETIC FRACTURE.
Patient problems: Bone Fracture(s); Fall
MAUDE report 21770077 ↗InjuryDec 30, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TOPATIENT FELL WENT TO EXPERT HIP.
Patient problems: Fall
MAUDE report 21044902 ↗InjuryMay 15, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryAug 14, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJun 29, 2022Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO FALL AND BROKE FEMUR.
Patient problems: Bone Fracture(s); Fall
MAUDE report 14856590 ↗InjuryJun 17, 2021Appropriate Device Problem Term/Code Not Available
InjuryApr 7, 2021Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - LOOSENING OF STEM.
Patient problems: Insufficient Information
MAUDE report 11627691 ↗InjuryMar 5, 2021Fracture
REVISION SURGERY - PATIENT FRACTURED FEMUR A MONTH POST OPERATION. HEAD, STEM, AND LINER WERE REMOVED. LINER REPLACED WITH 10 DEGREE HOODED DJO LINER, BUT BIOMET WAS USED FOR STEM.
Patient problems: Failure of Implant
MAUDE report 11423591 ↗InjurySep 14, 2020Adverse Event Without Identified Device or Use Problem
InjuryFeb 28, 2020Device Dislodged or Dislocated
REVISION SURGERY: THE PATIENT SUSTAINED AN INJURY POSTOPERATIVE. THIS CAUSED THE STEM TO SUBSIDE.
Patient problems: Injury
MAUDE report 9769411 ↗InjuryMay 14, 2019Device Dislodged or Dislocated
REVISION SURGERY - DUE TO THE PATIENT FALLING AND DISLOCATING.
Patient problems: Fall
MAUDE report 8609285 ↗InjuryMay 13, 2019Device Slipped
REVISION SURGERY - DUE TO THE STEM SUBSIDING CAUSING INSTABILITY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8605530 ↗
Other Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer devices
- Novation 134-36-45Exactech, Inc. · Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer2 recalls0 reports
- PINNACLE 1218-28-650Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer89 reports
- Trident 690-00-28FHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall37 reports
- Trident 690-00-22EHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall36 reports
- PINNACLE 1218-32-652Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer75 reports
- Trident 690-00-22DHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall22 reports
- PINNACLE 1218-32-654Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer70 reports
- Trident 69-2850Howmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall11 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page