NA 9751-90-000Recalls & reported problems
Depuy International Ltd · NECK RESECTION CALIPER · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295251422), received between Jun 22, 2022 and Jan 21, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (5 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
- Detachment of Device or Device Component5
- Break1
- Illegible Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 21, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT DURING A LOAN KIT INSPECTION BY THE LOAN KIT TECHNICIAN, THE C STEM NECK RESECTION CALIPER WAS FOUND TO HAVE A MISSING PART. NO SURGEON, PROCEDURE, OR PATIENT DETAILS ARE AVAILABLE AND NO FURTHER INFORMATION CAN BE OBTAINED BECAUSE THE CUSTOMER DID NOT REPORT THE CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24136413 ↗MalfunctionApr 21, 2025Break; Illegible Information; Break; Illegible Information
IT WAS REPORTED THAT A HIP CALIPER WAS BROKEN AND WORN. THE NUMBERS ARE WORN AND NOT ABLE TO BE READ. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21872637 ↗MalfunctionNov 22, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT DURING LOAN KIT INSPECTION, BY THE LOAN KIT TECHNICIAN IT WAS IDENTIFIED THAT THE INSTRUMENT IS MISSING THE LOCKING SCREW TO KEEP IT FROM SLIDING. THERE IS NO SURGEON, PROCEDURE, OR PATIENT DETAILS AVAILABLE. NO FURTHER INFORMATION CAN BE OBTAINED AS THE CASE WAS NOT REPORTED BY THE CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20759780 ↗MalfunctionMay 9, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT ONE OF THE PIECES IS MISSING FROM DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16895233 ↗MalfunctionApr 19, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT ONE OF THE PIECES IS MISSING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16768806 ↗MalfunctionJun 22, 2022Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT, A NECK RESECTION CALIPER IS MISSING THE SCREW FROM THE TOP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14778500 ↗
Other CALIPER devices
- JOURNEY 74014466Smith & Nephew, Inc. · CALIPER2 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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