Skip to content

LENS 72204685SRecalls & reported problems

Smith & Nephew, Inc. · SERVICE REPLACEMENT LENS INTEGRATED SYSTEM NON-WIFI VERSION · Class 2

All models of LENS (8)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556632024), received between Aug 16, 2020 and Aug 16, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “No Display/Image” (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

  • No Display/Image1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 16, 2020No Display/Image; No Display/Image

    IT WAS REPORTED THAT DURING A KNEE PROCEDURE, THERE WAS NO SIGNAL FROM THE DVI PORT OF THE LENS INTEGRATED SYSTEM. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITHOUT DELAY USING A BACK-UP DEVICE. NO PATIENT INJURY OR OTHER COMPLICATIONS WERE REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10411947 ↗

Other Laparoscope, general & plastic surgery devices

All Laparoscope, general & plastic surgery devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page