Anato 4845-7-115Recalls & 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
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613252631170), received between Mar 8, 2018 and Apr 11, 2019 — classified as 3 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
- Failure to Osseointegrate1
Patient problems
- Injury3
- Bone Fracture(s)2
- Inadequate Osseointegration1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryApr 11, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
SURGEON COMMENTED THAT THE GREATER TROCHANTER FRACTURED THROUGH THE INSERTION SITE OF THE PROXIMAL CHECKPOINT DURING THE JOINT REDUCTION WITH STEM IMPLANT AND TRIAL HEAD DURING MAKO DIRECT ANTERIOR APPROACH THA. THE SURGEON ALSO COMMENTED THAT HE DID NOT BELIEVE THAT THE CHECKPOINT CAUSED THE FRACTURE. THE FRACTURE WAS REPAIRED WITH A CERCLAGE CABLE. SURGICAL DELAY: 16-30 MINUTES.
Patient problems: Bone Fracture(s); Injury
MAUDE report 8503625 ↗InjuryAug 31, 2018Insufficient Device Problem Information; Insufficient Device Problem Information
RIGHT HIP REVISION, DUE TO PERIPROSTHETIC FRACTURE.
Patient problems: Bone Fracture(s); Injury
MAUDE report 7838400 ↗InjuryMar 8, 2018Failure to Osseointegrate; Failure to Osseointegrate
IT WAS REPORTED THAT PATIENT'S RIGHT HIP WAS REVISED DUE TO LACK OF ONGROWTH OF THE STEM (SURGEON REPORTED GROWTH WAS FIBROUS). THE STEM, HEAD, AND INSERT WERE REVISED BUT THE WELL-FIXED, WELL-POSITIONED CUP REMAINED.
Patient problems: Inadequate Osseointegration; Injury
MAUDE report 7324186 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page