Anato 4845-7-116Recalls & reported problems
Howmedica Osteonics Corp. · NEUTRAL 130 Degree Neck Angle V40 Hip Stem · Class 2 · Implant
All models of Anato (13)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613252631163), received between Sep 14, 2017 and Jul 17, 2018 — classified as 2 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 16, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information2
Patient problems
- Bone Fracture(s)2
- Injury2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 17, 2018Insufficient Device Problem Information; Insufficient Device Problem Information
SURGEON REPORTS PATIENT - A STATUS POST RIGHT TOTAL HIP DONE ON (B)(6) 2018 - FELT THE HIP CRACK WENT TO THE EMERGENCY ROOM, WHERE IT WAS DISCOVERED TO HAVE A PERI PROSTHETIC FRACTURE OF THE FEMORAL STEM. SURGEON DECIDED TO REVISE TO A RESTORATION MODULAR STEM. THE SURGERY WAS PERFORMED PER REST MOD SURGICAL TECHNIQUE. FOUR CABLES WERE PLACED TO REDUCE THE FRACTURE. A NEW 10 DEGREE HOODED LINER WAS IMPLANTED, AS WELL AS A NEW BIOLOX 36MM HEAD. THE SURGERY WAS PERFORMED WITHOUT INCIDENT.
Patient problems: Bone Fracture(s); Injury
MAUDE report 7695428 ↗InjurySep 14, 2017Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT A SURGEON REVISED PATIENT'S RIGHT HIP DUE TO PERIPROSTHETIC FRACTURE.
Patient problems: Bone Fracture(s); Injury
MAUDE report 6865441 ↗
Other Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate devices
- Novation 130-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls156 reports
- Novation 130-36-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls79 reports
- CORAIL 3L92511Depuy (Ireland) · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate158 reports
- Acumatch A Series 138-36-29Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate3 recalls1 report
- Novation 136-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls43 reports
- Novation 130-32-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls33 reports
- Novation 132-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls26 reports
- Novation 136-36-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls22 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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