Skip to content

MICROTEK 1 (UDI 00748426010370)Recalls & reported problems

Microtek Medical LLC · INTRAOPERATIVE PROBE COVER FEATURING ISOSILK, 1-EACH · Class 2

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 00748426010370), received between May 17, 2018 and May 17, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Hole In Material” (1 report).

8 other recalls cover devices cleared under the same FDA submission (K882724); they may or may not involve this specific model.

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

  • Hole In Material1
  • Material Rupture1

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.

  • MalfunctionMay 17, 2018Hole In Material; Material Rupture; Hole In Material; Material Rupture

    WHEN USING INTRAOPERATIVE PROVE COVER ON VASCULAR ULTRASOUND STERILE PROBE COVER SEPARATED WHILE IN USE ON PATIENT. SURGEON NOTIFIED AND INTRAOPERATIVE BACITRACIN ANTIBIOTIC WAS USED FOR IRRIGATION.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7522237 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K882724. One submission often covers many models, so check the product and lot details in each record.

  • Z-0753-2017 · Nov 30, 2016 · Terminated
    Ecolab, Microtek Rolled Probe Cover PC0907NB, Rx Only.
  • Z-0974-2014 · Jul 12, 2013 · Terminated
    5 x 93 US Probe Cover CMS-6049, Sterile, Single Patient Use. Custom Medical Specialties, Inc., Pine Level, NC, Federal (USA) law restricts this device to the sale by or on the orde
  • Z-0943-2014 · Jul 2, 2013 · Terminated
    MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER, featuring IsoSilk(R), 13cm x 244 cm, 5" x 96", REF PC3688N, QTY 100, Microtek Medical, Inc., Columbus, MS 39702.
  • Z-0946-2014 · Jul 2, 2013 · Terminated
    MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL, featuring IsoSilk(R), 5" x 98", (13cm x 249 cm), REF 3688, STERILE EO, QTY 20, Microtek Medical, Inc., Columbus, MS 39702
  • Z-0945-2014 · Jul 2, 2013 · Terminated
    MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL, featuring IsoSilk(R), 13cm x 244 cm, 5" x 96", REF PC3688EU, STERILE EO, QTY 20, Microtek Medical, Inc., Columbus, MS
  • Z-0947-2014 · Jul 2, 2013 · Terminated
    MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL, featuring IsoSilk(R), 13cm x 249 cm, REF 3688UK, STERILE EO, QTY 20, Microtek Medical, Inc., Columbus, MS 39702
  • Z-0948-2014 · Jul 2, 2013 · Terminated
    Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER, BUR HOLE COVER, 5 x 96, REF VPC0699, STERILE EO, QTY 20, Manufactured for Vital Care Reps, Inc., Tinley Park, Illinois
  • Z-0944-2014 · Jul 2, 2013 · Terminated
    MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER WITH GEL, featuring IsoSilk(R), 13cm x 244 cm, 5" x 96", REF PC3688, STERILE EO, QTY 20, Microtek Medical, Inc., Columbus, MS

Other Drape, surgical devices

All Drape, surgical devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.