Viant Medical, LLC T17617Recalls & reported problems
Viant Medical · CROSSBACK ACETABULAR REAMER 48 mm · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00840096400557), received between Jan 9, 2024 and Dec 13, 2024 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (6 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Cut6
- Adverse Event Without Identified Device or Use Problem5
- Degraded1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 13, 2024Degraded; Material Integrity Problem; Degraded; Material Integrity Problem
IT WAS REPORTED DURING AN UNKNOWN PROCEDURE ON A 76 YEAR OLD FEMALE PATIENT THAT THE REAMER WAS DULL. ADDITIONAL INFORMATION RECEIVED LATER INDICATED THE MALFUNCTION OCCURRED WHILE REAMING THE ACETABULUM AND THE CUP WOULD NOT SEAT. THEREFORE, THE CUP WAS TAKEN OUT TO REAM AGAIN PRESSING HARDER INTO THE ACETABULUM. THERE WAS A SLIGHT SURGICAL DELAY (COUPLE OF MINUTES) WITH NO CONSEQUENCES OR IMPACT TO PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20921978 ↗MalfunctionJan 9, 2024Failure to Cut; Adverse Event Without Identified Device or Use Problem; Failure to Cut; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT REAMER IS 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 PROPERT
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18480975 ↗MalfunctionJan 9, 2024Failure to Cut; Adverse Event Without Identified Device or Use Problem; Failure to Cut; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT REAMER IS 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)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEV
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18480971 ↗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 18480838 ↗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 18480829 ↗MalfunctionJan 9, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT 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)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PROPERTY OF -->NONE, DEVICE IN POSSESSION OF -->NONE, (B)(6) DEVICE PRO
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18479187 ↗MalfunctionJan 9, 2024Failure to Cut; Adverse Event Without Identified Device or Use Problem; Failure to Cut; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT 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, DEVIC
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18479101 ↗
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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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