VitalRecalls & reported problems across all models
Zimmer Biomet Inc · 4 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 13
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 4 models of Vital by Zimmer Biomet Inc in the FDA's device registry (GUDID). Together they are named in 13 adverse event reports in the FDA's MAUDE database, received between Feb 2, 2021 and Feb 18, 2025 — classified as 13 malfunctions.
The most frequently reported specific device problem is “Fracture” (6 reports).
1 FDA recall record name at least one of these models by its device identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Vital recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- May 5, 2020Class IITerminated
There are reports of inadequate locking of the extended tab screws. Complaints were reported where the closure top backed out of the screw post-operatively.
Z-2233-2020 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported Vital problems
Device problems
- Fracture6
- Material Twisted/Bent4
- Material Deformation3
- Inadequate User Interface1
- Naturally Worn1
Patient problems
- No Clinical Signs, Symptoms or Conditions12
- No Consequences Or Impact To Patient1
Vital models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Vital™ 850M0055Orthopedic Manual Surgical Instrument1 recall0 reports
- Vital™ 730M0060Screwdriver11 reports
- Vital™ 730M0050Screwdriver1 report
- Vital™ 850M3000Orthopedic Manual Surgical Instrument1 report
Recent Vital adverse event reports
The 13 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionFeb 18, 2025Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT A VITALITY DRIVER WITH A TWISTED TIP WAS DISCOVERED DURING PRE-INSPECTION. THERE WAS NO PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21406545 ↗MalfunctionDec 12, 2024Material Deformation; Material Deformation
IT WAS REPORTED THAT WHEN RE-INTRODUCING ILIAC SCREWS INTRA-OPERATIVELY, THROUGH FORCE, THE TIPS ON TWO VITAL CANNULATED DRIVERS BECAME DEFORMED. THEY DID NOT FRACTURE. THERE WAS NO PATIENT HARM. THIS IS REPORT ONE OF TWO FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20916951 ↗MalfunctionDec 12, 2024Material Deformation; Material Deformation
IT WAS REPORTED THAT WHEN RE-INTRODUCING ILIAC SCREWS INTRA-OPERATIVELY, THROUGH FORCE, THE TIPS ON TWO VITAL CANNULATED DRIVERS BECAME DEFORMED. THEY DID NOT FRACTURE. THERE WAS NO PATIENT HARM. THIS IS REPORT TWO OF TWO FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20914865 ↗MalfunctionNov 20, 2024Material Deformation; Material Deformation
IT WAS REPORTED THAT DURING SURGERY, A VITALITY STANDARD CANNULATED DRIVER WOULD NOT ENGAGE THE SCREW DUE TO TIP DEFORMATION. A SECOND DRIVER WAS USED AND THERE WAS NO IMPACT TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20737849 ↗MalfunctionSep 11, 2024Fracture; Fracture
IT WAS REPORTED THAT A VITAL MIS STANDARD CANNULATED DRIVER TIP FRACTURED INTRA-OPERATIVELY. ANOTHER DRIVER WAS USED TO COMPLETE THE PROCEDURE WITHOUT PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20192113 ↗MalfunctionJul 10, 2024Fracture; Material Twisted/Bent; Fracture; Material Twisted/Bent
IT WAS REPORTED THAT TWO VITALITY CANNULATED DRIVERS AND A VITALITY T27 CLOSURE TOP INSERTER FRACTURED INTRA-OPERATIVELY WHILE DRIVING A SCREW, BUT THAT THESE FRACTURES RESULTED IN NO PROCEDURAL DELAYS OR IMPACT TO THE PATIENT. IT WAS REPORTED THAT THE TIPS HAD BECOME TWISTED AND COMPROMISED OVER USE AND TIME. NO ADDITIONAL INSTRUMENTATION WAS REQUIRED TO COMPLETE THE SURGERY AND ALL PIECES WERE REMOVED PRIOR TO ROD INSERTION. THIS IS REPORT ONE OF THREE FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19716308 ↗MalfunctionJul 10, 2024Fracture; Material Twisted/Bent; Fracture; Material Twisted/Bent
IT WAS REPORTED THAT TWO VITALITY CANNULATED DRIVERS AND A VITALITY T27 CLOSURE TOP INSERTER FRACTURED INTRA-OPERATIVELY WHILE DRIVING A SCREW, BUT THAT THESE FRACTURES RESULTED IN NO PROCEDURAL DELAYS OR IMPACT TO THE PATIENT. IT WAS REPORTED THAT THE TIPS HAD BECOME TWISTED AND COMPROMISED OVER USE AND TIME. NO ADDITIONAL INSTRUMENTATION WAS REQUIRED TO COMPLETE THE SURGERY AND ALL PIECES WERE REMOVED PRIOR TO ROD INSERTION. THIS IS REPORT THREE OF THREE FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19716085 ↗MalfunctionJun 18, 2024Naturally Worn; Naturally Worn
IT WAS REPORTED THAT A VITALITY DRIVER IS WORN DUE TO USAGE. MANUFACTURER INSPECTION ALSO REVEALED THAT THE TIP OF THE DRIVER IS DEFORMED AND UNABLE TO MATE WITH A SCREW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19560354 ↗MalfunctionOct 21, 2021Fracture; Fracture
IT WAS REPORTED THE TIPS OF TWO CANNULATED DRIVERS BROKE WHILE IMPLANTING SCREWS IN THE PELVIS. THE TIPS WERE RETRIEVED. THERE WAS NO REPORTED PATIENT HARM. THIS IS REPORT TWO OF TWO FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12677740 ↗MalfunctionOct 21, 2021Fracture; Fracture
IT WAS REPORTED THE TIPS OF TWO CANNULATED DRIVERS BROKE WHILE IMPLANTING SCREWS IN THE PELVIS. THE TIPS WERE RETRIEVED. THERE WAS NO REPORTED PATIENT HARM. THIS IS REPORT ONE OF TWO FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12677739 ↗MalfunctionSep 10, 2021Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE TIP OF A DRIVER WAS FOUND TWISTED INTRA-OPERATIVELY; IT MAY HAVE BEEN DAMAGED DURING A PRIOR PROCEDURE. ANOTHER DRIVER WAS USED TO COMPLETED THE PROCEDURE WITHOUT PATIENT IMPACTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12452721 ↗MalfunctionMar 26, 2021Inadequate User Interface; Inadequate User Interface
IT WAS REPORTED THAT A TAP DID NOT PROVIDE TACTILE FEEDBACK FOR THE SURGEON TO GAUGE DEPTH WITH DURING SURGERY. HOWEVER, DEVICE EVALUATION BY THE MANUFACTURER FOUND THAT THE TAP WAS FRACTURED. THERE WERE NO PATIENT IMPACTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11577744 ↗MalfunctionFeb 2, 2021Fracture; Fracture
IT WAS REPORTED THAT A CLOSURE TOP STARTER FRACTURED INTRA-OP. A DIFFERENT DRIVER WAS USED TO COMPLETE THE CASE WITHOUT PATIENT IMPACTS.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 11268046 ↗
Other Zimmer Biomet Inc products
All Zimmer Biomet Inc devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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