SMALL CANNULATED SCREWS 71103340SRecalls & reported problems
Smith & Nephew, Inc. · 3.0MM HEADLESS CANNULATED SCREW 40MM STERILE · Class 2 · Implant
All models of SMALL CANNULATED SCREWS (18)
Data updated Oct 16, 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 03596010623713), received between Aug 20, 2024 and Aug 20, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Material Deformation” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Deformation1
Patient problems
- Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 20, 2024Material Deformation; Material Deformation
IT WAS REPORTED THAT DURING SURGERY, A 1.0 GUIDE WAS PLACED AND DRILLED, BUT THE 2.0MM CANN DRILL BIT W/QC OPENED AT THE TIP. THE DRILL BIT WAS CHANGED AND THE DRILLING WAS FINISHED, THE 3.0MM HEADLESS CANNULATED SCREW 40MM WAS PASSED, HOWEVER, IT WAS TOO LONG. WHEN CHANGING IT FOR A 34 SCREW CAME OUT OPEN AS WELL AS THE DRILL BIT. SURGERY WAS PERFORMED, AFTER A NON-SIGNIFICANT DELAY, WITH A BACK-UP DEVICE, PERFORMING AN ADDITIONAL BONE HOLE. THE PATIENT'S HEALTH WAS NOT AFFECTED.
Patient problems: Perforation
MAUDE report 20001621 ↗
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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.
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