Vitality® 07.02067.001Recalls & reported problems
Zimmer Spine, Inc. · Class 1
All models of Vitality (11)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024009912), received between Sep 12, 2019 and Apr 4, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (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 18, 2026.
Most reported problems
Device problems
- Fracture2
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 4, 2023Fracture; Fracture
IT WAS REPORTED, THE TIP OF A VITALITY STRAIGHT PEDICLE PROBE BROKE OFF IN THE PATIENT'S VERTEBRAL BODY INTRA-OPERATIVELY, WHILE THE SCREW HOLE WAS BEING PREPARED. THE FRACTURED PIECE WAS RECOVERED USING ANOTHER INSTRUMENT. AND THE PROCEDURE WAS COMPLETED WITHOUT PATIENT IMPACTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16676951 ↗MalfunctionSep 12, 2019Fracture; Fracture
IT WAS REPORTED THAT THE TIP OF THE PROBE BROKE AND WAS STUCK IN THE PEDICLE. THE TIP WAS RETRIEVED. ADDITIONAL BONE WAS REMOVED AROUND THE TIP IN ORDER TO REMOVE IT, BUT THERE WERE NO CHANGES TO THE PLANNED TREATMENT AND THERE WERE NO REPORTED PATIENT IMPACTS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9009540 ↗
Other PROBE devices
- EXPEDIUM 279702030Depuy Spine, LLC · PROBE53 reports
- Sklar 96-2361Sklar Corporation · PROBE1 recall0 reports
- Sklar Instruments 94-5923Sklar Corporation · PROBE1 recall0 reports
- MOSS 275010140Depuy Spine, LLC · PROBE28 reports
- EXPEDIUM 279702040Depuy Spine, LLC · PROBE21 reports
- MULTILOC 03.019.029Synthes GmbH · PROBE15 reports
- MOSS 275010160Depuy Spine, LLC · PROBE11 reports
- EXPEDIUM 279702010Depuy Spine, LLC · PROBE9 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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