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MICROTEK 1 (UDI 00748426007752)Recalls & reported problems

Microtek Medical LLC · CLOSED SYSTEM VIDEO CAMERA DRAPE W/2.54 CM DIAMETER LENS, 1-EACH · Class 2

Data updated Oct 13, 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 00748426007752), received between Oct 11, 2022 and Oct 11, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Entrapment of Device” (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

  • Entrapment of Device1

Patient problems

  • Device Embedded In Tissue or Plaque1

Recent adverse event reports

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

  • InjuryOct 11, 2022Entrapment of Device; Entrapment of Device

    IT WAS REPORTED THAT A FOREIGN BODY, PRESUMED TO BE TAPE FROM THE CAMERA DRAPE, WAS RETAINED IN THE PATIENT. INTERVENTION WAS REQUIRED TO REMOVE THE RETAINED FOREIGN BODY FROM THE PATIENT. NO PATIENT INJURY OR INFECTION RESULTING FROM THE RETAINED FOREIGN BODY WAS REPORTED.

    Patient problems: Device Embedded In Tissue or Plaque

    MAUDE report 15583892 ↗

Other Drape, surgical devices

All Drape, surgical devices →

Sources and updates

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