Peri-Loc 71173501Recalls & reported problems
Smith & Nephew, Inc. · 2.0MM DRILL BIT W/QUICK CONNECT · Class 2
All models of Peri-Loc (102)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03596010519696), received between Mar 25, 2019 and Dec 30, 2020 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (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 16, 2026.
Most reported problems
Device problems
- Break2
- Fracture1
- Peeled/Delaminated1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 30, 2020Break; Peeled/Delaminated; Break; Peeled/Delaminated
IT WAS REPORTED THAT THE 2.0MM DRILL W/QC IS DELAMINATED AND COMING APART. IT IS UNKNOWN WHERE THE EVENT OCCURS AND IF THERE WAS A PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11094787 ↗InjuryMar 25, 2019Break; Fracture; Break; Fracture
IT WAS REPORTED THAT DURING SURGERY THE TIP OF THE DRILL BROKE AND WAS LEFT IN THE PATIENT IN THE HUMERAL CANAL DUE TO THE SURGEON DECIDED THAT IT COULD CAUSE MORE DAMAGE TO RETRIEVE THE BROKEN PIECE THAN LEFT IT INSIDE THE PATIENT. THE SURGERY CONTINUED WITHOUT DELAY WITH A REPLACEMENT S&N DRILL BIT AND THE FINAL OUTCOME OF THE PATIENT WAS GREAT.
Patient problems: Foreign Body In Patient; No Consequences Or Impact To Patient
MAUDE report 8448489 ↗
Other PLATE, FIXATION, BONE devices
- Lapiplasty System 2 SK14Treace Medical Concepts, Inc. · Plate, Fixation, Bone260 reports
- PRECICE® Plating System LP4.5-PRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls6 reports
- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive 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-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PRT42Nuvasive 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 16, 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