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Viant Medical, LLC T17618Recalls & reported problems

Viant Medical · CROSSBACK ACETABULAR REAMER 49 mm · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00840096400564), received between Jan 9, 2024 and Jan 9, 2024 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Failure to Cut” (4 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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 4 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520264
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem4
  • Failure to Cut4

Patient problems

  • No Clinical Signs, Symptoms or Conditions4

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 9, 2024Failure to Cut; Adverse Event Without Identified Device or Use Problem; Failure to Cut; Adverse Event Without Identified Device or Use Problem

    ACETABULAR GRATERS HAVE BECOME DULL PATIENT STATUS/ OUTCOME / CONSEQUENCES NO PATIENT INVOLVEMENT, WAS OTHER MEDICAL INTERVENTION (E.G. X-RAYS, ADDITIONAL PROCEDURES, PRESCRIPTIONS, OTC, REVISION) REQUIRED: UNKNOWN, IS THE PATIENT PART OF A CLINICAL STUDY UNKNOWN, IP-01937713 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937714 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937715 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937716 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937717 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937718 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937719 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937720 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937721 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937722 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937723 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937724 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937725 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE, IP-01937726 DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NON

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18480825 ↗
  • MalfunctionJan 9, 2024Failure to Cut; Adverse Event Without Identified Device or Use Problem; Failure to Cut; Adverse Event Without Identified Device or Use Problem

    ACETABULAR GRATERS HAVE BECOME DULL. PATIENT STATUS/ OUTCOME / CONSEQUENCES --> NO PATIENT INVOLVEMENT, WAS OTHER MEDICAL INTERVENTION (E.G. X-RAYS, ADDITIONAL PROCEDURES, PRESCRIPTIONS, OTC, REVISION) REQUIRED: --> UNKNOWN, IS THE PATIENT PART OF A CLINICAL STUDY --> UNKNOWN, IP-01937713 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937714 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937715 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937716 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937717 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937718 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937719 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937720 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937721 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937722 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937723 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937724 DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, IP-01937725 DEVICE PROPERTY OF -->NONE, DEVICE

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18480823 ↗
  • MalfunctionJan 9, 2024Failure to Cut; Adverse Event Without Identified Device or Use Problem; Failure to Cut; Adverse Event Without Identified Device or Use Problem

    ACETABULAR GRATERS HAVE BECOME DULL. PATIENT STATUS/ OUTCOME / CONSEQUENCES --> NO PATIENT INVOLVEMENT, WAS OTHER MEDICAL INTERVENTION (E.G. X-RAYS, ADDITIONAL PROCEDURES, PRESCRIPTIONS, OTC, REVISION) REQUIRED: --> UNKNOWN, IS THE PATIENT PART OF A CLINICAL STUDY --> UNKNOWN, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(4), DEVICE PROPERTY O

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18480822 ↗
  • MalfunctionJan 9, 2024Failure to Cut; Adverse Event Without Identified Device or Use Problem; Failure to Cut; Adverse Event Without Identified Device or Use Problem

    ACETABULAR GRATERS HAVE BECOME DULL. PATIENT STATUS/ OUTCOME / CONSEQUENCES: NO PATIENT INVOLVEMENT. WAS OTHER MEDICAL INTERVENTION (E.G. X-RAYS, ADDITIONAL PROCEDURES, PRESCRIPTIONS, OTC, REVISION) REQUIRED? UNKNOWN. IS THE PATIENT PART OF A CLINICAL STUDY? UNKNOWN. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE., (B)(4). DEVICE PROPERTY OF: NONE. DEVICE IN POSSESSION OF: NONE. (B)(4). DEVICE PROPER

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18480820 ↗

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Sources and updates

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