VLP FOOT 72823112SRecalls & reported problems
Smith & Nephew, Inc. · VLP 2.7MM SELF-TAPPING LOCKING CORTEX SCREW 12MM STERILE · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03596010649300), received between Jun 7, 2021 and Jun 7, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Connection Problem” (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 18, 2026.
Most reported problems
Device problems
- Connection Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 7, 2021Connection Problem; Connection Problem
IT WAS REPORTED THAT, VLP 2.7MM S-T LOCK CORT SCR 12MM STER SCREWS WERE NOT LOCKING. IT WAS UNKNOWN IF THIS OCCURRED DURING SURGERY OR NOT; THEREFORE, PATIENT INVOLVEMENT HAS NOT BEEN CONFIRMED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11952309 ↗MalfunctionJun 7, 2021Connection Problem; Connection Problem
IT WAS REPORTED THAT, VLP 2.7MM S-T LOCK CORT SCR 12MM STER SCREWS WERE NOT LOCKING. IT WAS UNKNOWN IF THIS OCCURRED DURING SURGERY OR NOT; THEREFORE, PATIENT INVOLVEMENT HAS NOT BEEN CONFIRMED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11952293 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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