NOVO Health Services, LLC 2314Recalls & reported problems
Novo Health Services, LLC · Towel, 12-Pack (FF) · Class 1
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 00812564036889), received between Oct 28, 2019 and Oct 28, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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
- Contamination /Decontamination Problem1
- Device Reprocessing Problem1
- Failure to Clean Adequately1
Patient problems
- Missing Value Reason1
- 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.
MalfunctionOct 28, 2019Device Reprocessing Problem; Contamination /Decontamination Problem; Failure to Clean Adequately; Device Reprocessing Problem; Contamination /Decontamination Problem; Failure to Clean Adequately
THE USER FACILITY REPORTED THAT WHILE THE SURGICAL TECHNICIAN AND THE DOCTOR WERE DRAPING THE PATIENT WITH REUSABLE STERILE TOWELS A RAYTEX FELL OUT OF THE TOWEL AND LANDED ON THE PATIENT. THE RAYTEX COUNT WAS PREFORMED TO VERIFY THAT THE SPONGE WAS "EXTRA."
Patient problems: Missing Value Reason; No Known Impact Or Consequence To Patient
MAUDE report 9244413 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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