Continuum Trilogy Allofit Vivacit-ERecalls & reported problems across all models
Zimmer, Inc. · 18 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 25
- Deaths reported
- 0
- Injuries reported
- 14
- Recalls
- 0
We found 18 models of Continuum Trilogy Allofit Vivacit-E by Zimmer, Inc. in the FDA's device registry (GUDID). Together they are named in 25 adverse event reports in the FDA's MAUDE database, received between Dec 12, 2019 and Jun 17, 2026 — classified as 14 injuries, 11 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (9 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. 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
Most reported Continuum Trilogy Allofit Vivacit-E problems
Device problems
- Device Dislodged or Dislocated9
- Adverse Event Without Identified Device or Use Problem4
- Difficult to Insert4
- Device Contaminated During Manufacture or Shipping3
- Positioning Failure3
- Unstable2
- Fracture1
- Inadequacy of Device Shape and/or Size1
Patient problems
- Joint Dislocation9
- No Clinical Signs, Symptoms or Conditions7
- Pain5
- No Consequences Or Impact To Patient3
- No Known Impact Or Consequence To Patient3
- Tissue Damage2
- Loss of Range of Motion1
- Unspecified Infection1
Continuum Trilogy Allofit Vivacit-E models
18 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-007-28Hip, semi-constrained, cemented, metal/polymer + additive, cemented2 reports
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-008-32Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-009-32Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-010-36Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented2 reports
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-011-32Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-013-36Hip, semi-constrained, cemented, metal/polymer + additive, cemented2 reports
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8852-009-32PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-008-28Hip, semi-constrained, cemented, metal/polymer + additive, cemented1 report
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-011-36Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented1 report
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-012-40Hip, semi-constrained, cemented, metal/polymer + additive, cemented1 report
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-014-36Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-015-36Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 report
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8851-016-36Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8852-006-28Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented1 report
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8852-008-32Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8852-010-32Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 report
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8852-012-36Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented1 report
- Continuum® Trilogy® Allofit® Vivacit-E® 00-8852-014-36Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
Recent Continuum Trilogy Allofit Vivacit-E adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJun 17, 2026Device Dislodged or Dislocated
IT WAS REPORTED THE PATIENT EXPERIENCED A HIP DISLOCATION AND WAS REVISED APPROXIMATELY 4 MONTHS POST-IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Joint Dislocation
MAUDE report 25537367 ↗InjuryJul 28, 2025Inadequacy of Device Shape and/or Size; Device Dislodged or Dislocated; Inadequacy of Device Shape and/or Size; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO LINER DISLOCATION. THE WRONG LINER AND CUP SIZE WERE PLACED DURING THE INITIAL PROCEDURE.
Patient problems: Joint Dislocation
MAUDE report 22635467 ↗InjuryFeb 25, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.
Patient problems: Joint Dislocation
MAUDE report 21460308 ↗InjuryDec 2, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THERE IS NO UPDATE TO THE PRIOR EVENT DESCRIPTION PROVIDED.
Patient problems: Pain
MAUDE report 20820293 ↗InjuryAug 22, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.
Patient problems: Joint Dislocation
MAUDE report 20041033 ↗InjuryOct 2, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED BY THE SURGEON THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE AND WAS REVISED APPROXIMATELY SEVEN YEARS LATER DUE TO SUSPECTED WEAR OF THE LINER. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17852734 ↗MalfunctionSep 8, 2023Difficult to Insert; Difficult to Insert
THERE IS NO UPDATE TO THE PRIOR EVENT DESCRIPTION PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17711166 ↗InjurySep 6, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.
Patient problems: Joint Dislocation
MAUDE report 17694298 ↗MalfunctionJun 13, 2023Difficult to Insert; Difficult to Insert
THERE IS NO UPDATE TO THE PRIOR EVENT DESCRIPTION PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17119076 ↗MalfunctionJan 30, 2023Difficult to Insert; Difficult to Insert
NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16265066 ↗InjuryApr 15, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO PAIN AND POOR CUP POSITION APPROXIMATELY 2 YEARS POST IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.
Patient problems: Pain
MAUDE report 14117314 ↗MalfunctionAug 27, 2021Difficult to Insert; Difficult to Insert
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12376916 ↗InjuryApr 26, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Joint Dislocation; Pain
MAUDE report 11724123 ↗MalfunctionApr 1, 2021Device Contaminated During Manufacture or Shipping; Packaging Problem; Device Contaminated During Manufacture or Shipping; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11602558 ↗MalfunctionFeb 9, 2021Positioning Failure; Positioning Failure
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient
MAUDE report 11301532 ↗
Other Zimmer, Inc. products
- PERSONA364 models · 2,000 reports · 3 recalls
- Persona The Personalized Knee77 models · 1,396 reports
- PERSONA Vivacit-E285 models · 1,152 reports
- NexGen198 models · 842 reports · 4 recalls
- Affixus18 models · 1 reports · 17 recalls
- PERSONA Natural Tibia25 models · 417 reports · 2 recalls
- NexGen Legacy119 models · 319 reports · 3 recalls
- Alliance32 models · 275 reports · 2 recalls
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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