MICROTEK 1 (UDI 00748426076451)Recalls & reported problems
Microtek Medical LLC · GENERAL PURPOSE PROBE COVER · 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 00748426076451), received between Aug 18, 2017 and Aug 18, 2017 — 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
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 18, 2017Hole In Material; Hole In Material
THE END USER IS REPORTING: STERILE PROBE COVER USED TO COVER UNSTERILE PROBE DURING SURGERY. POST PROCEDURE WHEN PROBE COVER REMOVED THERE WAS BLOOD ON THE PROBE. ON INSPECTION BLOOD SEEPED THROUGH SEAMS AND MICRO HOLE IN COVER. NO VISIBLE HOLE PRESENT. THE SAME THING HAPPENED IN JUNE. ALL PROBE COVERS OF THAT LOT NUMBER ARE PULLED FROM SERVICE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6804885 ↗
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 · TerminatedEcolab, Microtek Rolled Probe Cover PC0907NB, Rx Only.
- Z-0974-2014 · Jul 12, 2013 · Terminated5 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 · TerminatedMICROTEK(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-0944-2014 · Jul 2, 2013 · TerminatedMICROTEK(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
- Z-0948-2014 · Jul 2, 2013 · TerminatedVital 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-0945-2014 · Jul 2, 2013 · TerminatedMICROTEK(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-0946-2014 · Jul 2, 2013 · TerminatedMICROTEK(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-0947-2014 · Jul 2, 2013 · TerminatedMICROTEK(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
Other Drape, surgical devices
- Medline DYNJP8002Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2414RMedline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2411Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2410Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2416Medline Industries, Inc. · Drape, surgical2 recalls1 report
- Medline DYNJP3008UGMedline Industries, Inc. · Drape, surgical2 recalls1 report
- Medline DYNJP8201UGMedline Industries, Inc. · Drape, surgical2 recalls0 reports
- Medline DYNJP2412TMedline Industries, Inc. · Drape, surgical2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.