DJO SURGICAL 425-99-009Recalls & reported problems
Encore Medical, L.P. · Linear, Lateral, Reduced Neck, Sz9, W/P2 Coating · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00888912078955), received between Feb 1, 2016 and Mar 2, 2026 — classified as 6 injuries.
The most frequently reported specific device problem is “Break” (2 reports).
1 other recall cover devices cleared under the same FDA submission (K120241); they may or may not involve this specific model.
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 Problem3
- Break2
- Appropriate Device Problem Term/Code Not Available1
- Fracture1
Patient problems
- Fall4
- Bone Fracture(s)3
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryMar 2, 2026Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT SUSTAINED A FALL THAT RESULTED IN A PERIPROSTHETIC FRACTURE OF THE FUMUR.
Patient problems: Bone Fracture(s); Fall
MAUDE report 24477770 ↗InjuryJun 26, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMay 20, 2021Adverse Event Without Identified Device or Use Problem
THIRD REVISION SURGERY - TOOK OUT FEMORAL HEAD AND STEM AND PUT IN EXPRT REVISION STEM WITH NEW FEMORAL HEAD.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11858476 ↗InjuryNov 19, 2019Break; Appropriate Device Problem Term/Code Not Available
InjuryJul 11, 2019Break
REVISION SURGERY - THE PATIENT FELL AND BROKE HER FEMUR.
Patient problems: Fall
MAUDE report 8783120 ↗InjuryFeb 1, 2016Fracture
REVISION SURGERY - DUE TO THE PATIENT FALLING AND SUSTAINING A PERIPROSTHETIC FRACTURE. THIS RESULTED IN THE USE OF A DISTAL FIXATION STEM, SO THE SURGEON USED A LIMA REVISION STEM. HE REMOVED ALL OF THE ORIGINAL IMPLANTS.
Patient problems: Bone Fracture(s); Fall
MAUDE report 5402454 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K120241. One submission often covers many models, so check the product and lot details in each record.
- Z-1692-2020 · Jul 10, 2018 · Open, Classifieddjosurgical Linear Neck Trials with Spring Sides, Standard, nonsterile, REF S-200635; and djosurgical Linear Neck Trials with Spring Sides, Lateral, nonsterile, REF S-200636. The
Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices
- BIOLOX DELTA 1365-32-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented551 reports
- PINNACLE ALTRX 1221-36-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented481 reports
- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
- BIOLOX DELTA 1365-36-720Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death189 reports
- DJO SURGICAL 400-03-362Encore Medical, L.P. · Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented187 reports
- Anthology 71365705Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented176 reports
- BIOLOX DELTA 1365-40-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented170 reports
- PINNACLE GRIPTION 1217-32-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented169 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.
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