IBS™ S25 ST024Recalls & reported problems
In2bones · IBS 2.5-C COMPRESSION SCREW, DIAM2.5 LG 24MM T7 · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03760225710159), received between Nov 12, 2020 and Nov 12, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (1 report).
3 other recalls cover devices cleared under the same FDA submission (K131920); they may or may not involve this specific model.
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Improper or Incorrect Procedure or Method1
Patient problems
- Device Embedded In Tissue or Plaque1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 12, 2020Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
THE I.B.S(R) COMPRESSION AND NEUTRALIZATION OSTEOSYNTHESIS SCREWS ARE INTENDED FOR: THE FIXATION OF ARTHRODESIS, OSTEOTOMIES OR FRACTURES OF LONG OR SHORT BONES OF THE UPPER AND LOWER LIMBS. OSTEOSYNTHESIS REQUIRING A MONO OR BICORTICAL COMPRESSION. EVENT DESCRIPTION: AN I.B.S COMPRESSION SCREW IS REPORTED TO HAVE BROKEN DURING A BUNION SURGERY (I.E. CORRECTION OF AN HALLUX VALGUS). DESPITE THE REPORTED PROBLEM, THE SURGERY ENDED SUCCESSFULLY WITHOUT ANY CONSEQUENCES FOR THE PATIENT.
Patient problems: Device Embedded In Tissue or Plaque; No Consequences Or Impact To Patient
MAUDE report 10827446 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K131920. One submission often covers many models, so check the product and lot details in each record.
- Z-1319-2024 · Jan 26, 2024 · Open, ClassifiedI.B.S 6.5-C Compression screw - diam 6.5mm lg 75mm,Part Number S65 ST175
- Z-1320-2024 · Jan 26, 2024 · Open, ClassifiedI.B.S 6.5-C Compression screw - diam 6.5mm lg 80mm,Part Number S65 ST180
- Z-0397-2016 · Nov 18, 2015 · TerminatedIBS - Osteosynthesis screws for bone fixation Model S25 ST014.
Other Screw, Fixation, Bone devices
- NA 03.043.029Synthes GmbH · Screw, fixation, bone503 reports
- OSTEORAPTOR 72201995Smith & Nephew, Inc. · Screw, fixation, bone253 reports
- Control 360 SK12Treace Medical Concepts, Inc. · Screw, Fixation, Bone195 reports
- HEALIX PEEK ORTHOCORD 222205Medos International Sàrl · Screw, fixation, bone186 reports
- PRECICE® Bone Transport System STP3.5-375Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-225Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-200Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page