IPS 60-000-72-09-LPRecalls & reported problems
KLS-Martin L.P. · IMPLANT, MIDFACE/ORTHOG, 00072, LP, TI-6AL-4V · Class 2 · Implant
All models of IPS (29)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00888118140425), received between Apr 30, 2025 and Jun 24, 2026 — classified as 6 injuries.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem4
- Fracture2
Patient problems
- Insufficient Information4
- Nonunion/Delayed-union Bone Fracture2
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryJun 24, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT AN IPS IMPLANT WAS REMOVED FOLLOWING APPROXIMATELY TWELVE MONTHS OF IMPLANTATION.
Patient problems: Insufficient Information
MAUDE report 25610344 ↗InjuryJun 24, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED AN IPS IMPLANT WAS REMOVED FOLLOWING APPROXIMATELY ONE MONTH OF IMPLANTATION.
Patient problems: Insufficient Information
MAUDE report 25610335 ↗InjuryDec 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IPS IMPLANTS WERE REMOVED DUE TO UNKNOWN REASONS.
Patient problems: Insufficient Information
MAUDE report 23855152 ↗InjuryDec 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT IPS IMPLANTS WERE REMOVED DUE TO UNKNOWN REASONS.
Patient problems: Insufficient Information
MAUDE report 23855129 ↗InjuryApr 30, 2025Fracture; Fracture
IT WAS REPORTED IPS PLATES WERE FOUND TO BE FRACTURED APPROXIMATELY 6 MONTHS POST PROCEDURE POSSIBLY DUE TO A MOBILE MAXILLA. IT WAS REMOVED AND REPLACED.
Patient problems: Nonunion/Delayed-union Bone Fracture
MAUDE report 21938472 ↗InjuryApr 30, 2025Fracture; Fracture
IT WAS REPORTED IPS PLATES WERE FOUND TO BE FRACTURED APPROXIMATELY 6 MONTHS POST PROCEDURE POSSIBLY DUE TO A MOBILE MAXILLA. IT WAS REMOVED AND REPLACED.
Patient problems: Nonunion/Delayed-union Bone Fracture
MAUDE report 21938470 ↗
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- RapidSorb 806.004.02SSynthes GmbH · PLATE, BONE146 reports
- TruMatch SD980.001Materialise NV · Plate, Bone1 recall21 reports
- Matrix 04.511.225.01Synthes GmbH · PLATE, BONE62 reports
- NA 400.834Synthes GmbH · PLATE, BONE58 reports
- TruMatch SD980.016Materialise NV · Plate, Bone55 reports
- ProPlan CMF SD900.101Materialise NV · Plate, Bone1 recall1 report
- TruMatch SD980.013Materialise NV · Plate, Bone1 recall0 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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