KinectivRecalls & reported problems across all models
Zimmer, Inc. · 21 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 50
- Deaths reported
- 0
- Injuries reported
- 38
- Recalls
- 0
We found 21 models of Kinectiv by Zimmer, Inc. in the FDA's device registry (GUDID). Together they are named in 50 adverse event reports in the FDA's MAUDE database, received between Dec 10, 2019 and Mar 2, 2026 — classified as 38 injuries, 12 malfunctions.
The most frequently reported specific device problem is “Fracture” (12 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 Kinectiv problems
Device problems
- Adverse Event Without Identified Device or Use Problem20
- Fracture12
- Material Erosion6
- Device Dislodged or Dislocated4
- Naturally Worn3
- Device Contaminated During Manufacture or Shipping2
- Unstable2
- Corroded1
Patient problems
- Pain14
- No Clinical Signs, Symptoms or Conditions12
- Bone Fracture(s)11
- Failure of Implant9
- Metal Related Pathology9
- Joint Dislocation8
- Muscle/Tendon Damage5
- Fall4
Kinectiv models
21 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Kinectiv® 00-7805-061-01ORTHOPEDIC MANUAL SURGICAL INSTRUMENT9 reports
- Kinectiv® 00-7713-009-00Prosthesis, hip, semi-constrained, metal/polymer, uncemented4 reports
- Kinectiv® 00-7848-002-00PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED4 reports
- Kinectiv® 00-7848-013-00PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED4 reports
- Kinectiv® 00-7713-012-00PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 reports
- Kinectiv® 00-7713-016-00Prosthesis, hip, semi-constrained, metal/polymer, uncemented3 reports
- Kinectiv® 00-7848-022-00Prosthesis, hip, semi-constrained, metal/polymer, uncemented3 reports
- Kinectiv® 00-7848-023-00PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 reports
- Kinectiv® 00-7713-006-00PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 reports
- Kinectiv® 00-7713-010-00Prosthesis, hip, semi-constrained, metal/polymer, uncemented2 reports
- Kinectiv® 00-7713-013-00Prosthesis, hip, semi-constrained, metal/polymer, uncemented2 reports
- Kinectiv® 00-7848-003-00Prosthesis, hip, semi-constrained, metal/polymer, uncemented2 reports
- Kinectiv® 00-7713-007-00PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Kinectiv® 00-7713-011-00PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Kinectiv® 00-7848-011-01Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 report
- Kinectiv® 00-7848-012-00Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 report
- Kinectiv® 00-7848-033-00Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 report
- Kinectiv® 00-7848-044-00PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Kinectiv® 00-7848-013-01Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 report
- Kinectiv® 00-7848-030-01PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- Kinectiv® 00-7848-032-01Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 report
Recent Kinectiv adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryMar 2, 2026Implant subsidence
IT WAS REPORTED, DURING THE REHABILITATION PERIOD, THE STEM SUBSIDENCE OCCURRED DUE TO A SKELETAL FRACTURE. IT WAS CONFIRMED THAT NO FURTHER INFORMATION COULD BE PROVIDED.
Patient problems: Bone Fracture(s)
MAUDE report 24481986 ↗InjuryNov 18, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT WAS REVISED APPROXIMATELY 1 WEEK LATER DUE TO DISLOCATION. ATTEMPTS HAVE BEEN MADE, AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Joint Dislocation
MAUDE report 23584629 ↗InjuryNov 18, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT WAS REVISED APPROXIMATELY 1 WEEK LATER DUE TO DISLOCATION. ATTEMPTS HAVE BEEN MADE, AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Joint Dislocation
MAUDE report 23584620 ↗MalfunctionNov 6, 2025Fracture; Fracture
NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23486727 ↗InjuryOct 24, 2025Material Erosion; Naturally Worn; Material Erosion; Naturally Worn
NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.
Patient problems: Joint Dislocation; Metal Related Pathology
MAUDE report 23377926 ↗InjuryOct 24, 2025Material Erosion; Naturally Worn; Material Erosion; Naturally Worn
NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.
Patient problems: Joint Dislocation; Metal Related Pathology
MAUDE report 23377922 ↗InjuryJun 26, 2025Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT THE PATIENT UNDERWENT A LEFT HIP REVISION APPROXIMATELY 10 YEARS POST IMPLANTATION DUE TO DISLOCATION. DURING THE PROCEDURE, THE CUP WAS FOUND TO BE MALPOSITIONED, AND THE TRUNNION OF THE NECK WAS IMPINGING ON THE POSTERIOR ELEVATED RIM OF THE ACETABULAR LINER. THE CUP WAS EXPLANTED, AND NEW CUP WAS IMPLANTED IN A BETTER POSITION. THE NECK WAS CHANGED AND ADJUSTED TO ACCOMMODATE THE NEW CUP POSITION. NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22336789 ↗MalfunctionMay 12, 2025Fracture; Fracture
IT WAS REPORTED THAT THE PLASTIC ON THE TIP OF THE STEM INSERTER WAS CRACKED. THERE WAS NO PATIENT INJURY AS A RESULT OF THE MALFUNCTION. THERE IS NO FURTHER INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22002141 ↗MalfunctionMay 8, 2025Fracture; Fracture
IT WAS REPORTED THAT THE BLUE COVER/ACCESSORIES AT THE FRONT ARE BROKEN OR DAMAGED. NO KNOWN IMPACT OR CONSEQUENCE TO THE PATIENT. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21987694 ↗MalfunctionApr 2, 2025Fracture; Fracture
IT WAS REPORTED THAT AFTER SURGERY, THE BLUE PLASTIC OF THE INSTRUMENT BROKE. THERE WAS NO PATIENT INVOLVEMENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21750657 ↗MalfunctionMar 20, 2025Fracture; Fracture
NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21652718 ↗MalfunctionMar 20, 2025Fracture; Fracture
IT WAS REPORTED THAT THE BLUE COVER ON THE STEM INSERTER IS BROKEN. THERE WAS NO KNOWN IMPACT OR CONSEQUENCES TO THE PATIENT. ATTEMPTS HAVE BEEN MADE, AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21652433 ↗InjuryMar 10, 2025Degraded; Adverse Event Without Identified Device or Use Problem; Degraded; Adverse Event Without Identified Device or Use Problem
NO FURTHER INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Unspecified Infection
MAUDE report 21558447 ↗InjuryDec 3, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT WAS REVISED APPROXIMATELY 3 MONTHS LATER DUE TO PERIPROSTHETIC FRACTURE FOLLOWING A FALL. DURING THE REVISION 5 CERCLAGE WIRES WERE USED TO REDUCE AND STABILIZE THE FRACTURE. THE STEM AND HEAD WERE REPLACED WITHOUT COMPLICATIONS. IT WAS REPORTED THAT NO FURTHER INFORMATION WAS AVAILABLE
Patient problems: Bone Fracture(s); Failure of Implant; Hematoma
MAUDE report 20835906 ↗MalfunctionNov 5, 2024Fracture; Fracture
NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20609008 ↗
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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