RibLoc RBP1132Recalls & reported problems
Acute Innovations LLC · 10mm x 76mm Rib Plate · Class 2
All models of RibLoc (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10814493010104), received between Aug 13, 2018 and Aug 13, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
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.
Most reported problems
Device problems
- Break1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 13, 2018Break; Break
PATIENT SUFFERED RIB FRACTURES IN 2012. RIBS 6&7 WERE PLATED. RECENTLY PATIENT REACHED DOWN TO PICK UP CHILD, FELT A POP AND PAIN IN LEFT RIB CASE. X-RAYS SHOW ORIGINAL FRACTURE TO HAVE HEALED. BROKEN PLATE AND ASSOCIATED SCREWS WERE REMOVED. PARTS WERE RETURNED FOR INVESTIGATION, NO OBVIOUS FAILURE MODE WAS IDENTIFIED. NORMAL WEAR FROM INSTALLATION AND REMOVAL WERE NOTED ON THE SCREWS. BROKEN PLATE ENDS WERE RUBBED SMOOTH FROM RUBBING, HOW LONG COULD NOT BE DETERMINED.
Patient problems: Failure of Implant
MAUDE report 7778554 ↗
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- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive Specialized Orthopedics, Inc. · Plate, 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 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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