ELEOS™ 25107000ERecalls & reported problems
Onkos Surgical, Inc. · TAPER DISASSEMBLY TOOL · Class 1
All models of ELEOS (127)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI B27825107000EE0), received between Feb 8, 2025 and Feb 8, 2025 — classified as 1 malfunction.
11 other recalls cover devices cleared under the same FDA submission (K161520); 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED BY (B)(4), AN ONKOS DISTRIBUTOR, THAT A 69-YEAR-OLD FEMALE PATIENT WITH AN ELEOS TOTAL FEMUR REPLACEMENT (TFR) UNDERWENT REVISION DUE TO THE CONSTRUCT BEING TOO LONG; THE PRESENCE OF CLINICAL SYMPTOMS IS UNKNOWN. DURING THE REVISION SURGERY, THE TAPER DISASSEMBLY TOOL REPORTEDLY BECAME STUCK DURING USE. THE SURGEON SUBSEQUENTLY DISENGAGED THE TFR CONSTRUCT FROM THE DUAL MOBILITY HEAD AND INSERTED A CEMENT SPACER. THERE WAS NO ALLEGED FAILURE OF THE EXPLANTED IMPLANTS TO PERFORM AS INTENDED; HOWEVER, A FOLLOW-UP SURGERY TO REPLACE THE PATIENT'S TFR CONSTRUCT WILL BE NECESSARY.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 21340557 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K161520. One submission often covers many models, so check the product and lot details in each record.
- Z-2423-2025 · Jul 11, 2025 · Open, ClassifiedELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS BOWED CANAL FILLING STEMS. Canal filling stem implants.
- Z-2425-2025 · Jul 11, 2025 · Open, ClassifiedELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS STEM EXTENSION, STRAIGHT, SPLINED, SLOTTED. Canal filling stem implants.
- Z-2424-2025 · Jul 11, 2025 · Open, ClassifiedELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING STRAIGHT SLOTTED SPLINED 2/3 PLASMA. Canal filling stem implants.
- Z-1857-2025 · Sep 22, 2024 · Open, ClassifiedELEOS MALE-FEMALE MIDSECTION 40MM. Part Number: 25001040E. Component of ELEOS Limb Salvage System
- Z-1884-2025 · Sep 1, 2023 · Open, ClassifiedMale-Female Midsection with the following sizes and model numbers. a. Male-Female Midsection, 40mm, 1 EACH; Model Number: 25001040E b. Male-Female Midsection, 50mm, 1 EACH; Model
- Z-1881-2025 · Sep 1, 2023 · Open, ClassifiedSegmental Stem, Canal Filling, Straight, 120MM, 1 EACH. Model Numbers: FS-11120-03M, FS-12120-03M, FS-13120-03M, FS-14120-03M, FS-15120-03M, FS-16120-03M, FS-17120-03M, FS-18120-03
- Z-1879-2025 · Sep 1, 2023 · Open, Classifieda. Segmental Stem, Cemented, Straight, 100MM, 1 EACH; Model Numbers: CS-09100-03M, CS-10100-03M. b. Segmental Stem, Cemented, Straight, 120MM, 1 EACH. Model Numbers: CS-11120-03M,
- Z-1882-2025 · Sep 1, 2023 · Open, ClassifiedSegmental Stem, Canal Filling, Bowed 152MM, 1 EACH. Model Numbers: FB-11152-03M, FB-12152-03M, FB-13152-03M, FB-14152-03M, FB-15152-03M, FB-16152-03M, FB-17152-03M, FB-18152-03M, F
- Z-2647-2017 · May 23, 2017 · TerminatedELEOS LIMB SALVAGE SYSTEM SEGMENTAL STEM, CANAL FILLING, DIAMETER 20MM, LENGTH 120MM, STYLE STRAIGHT, TYPE CANAL FILLING, COLLAR 25MM; REF 2500SP20E
- Z-2646-2017 · May 23, 2017 · TerminatedELEOS LIMB SALVAGE SYSTEM SEGMENTAL STEM, CANAL FILLING, DIAMETER 18MM, LENGTH 120MM, STYLE STRAIGHT, TYPE CANAL FILLING, COLLAR 25MM, REF 2500SP18E
- Z-2648-2017 · May 23, 2017 · TerminatedELEOS LIMB SALVAGE SYSTEM SEGMENTAL STEM, CANAL FILLING, DIAMETER 20MM, LENGTH 120MM, STYLE STRAIGHT, TYPE CANAL FILLING, COLLAR 25MM; REF 2500SP22E
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- EXPRESSEW 214141Medos International Sàrl · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1,166 reports
- N/A 9560524Medtronic Sofamor Danek, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT866 reports
- INHANCE 6500-11-104Depuy (Ireland) · Orthopedic manual surgical instrument831 reports
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- R3 71364450Smith & Nephew, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT520 reports
- N/A 9561524Medtronic Sofamor Danek, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT494 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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