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LITe DECOMPRESSION 48081805Recalls & reported problems

Stryker Corporation · TUBE · Class 1

Data updated Oct 13, 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 07613327264166), received between Oct 17, 2018 and Oct 17, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionOct 17, 2018Detachment of Device or Device Component

    IT WAS REPORTED THAT DURING A PROCEDURE, A CIRCULAR PART OF THE MIS DECOMPRESSION TUBE, INDICATING ITS LENGTH, CAME OFF INSIDE PATIENT. THIS DID NOT CAUSE AN ADVERSE CONSEQUENCE TO THE PATIENT, AND THE COMPONENT WAS SUCCESSFULLY REMOVED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7974727 ↗

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Sources and updates

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