Halyard 51739Recalls & reported problems
Avanos Medical, Inc. · HYH,DRAPE,VIDEO,5INX96IN,100 · Class 2
All models of Halyard (232)
Data updated Oct 16, 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 10680651517392), received between Jun 18, 2024 and Jun 18, 2024 — classified as 1 injury.
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 18, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
CUSTOMER REPORTED THAT THE NODE NAVIGATOR WAS PROPERLY DRAPED AND SECURED WITH VIDEO DRAPE. DURING RIGHT SEED LOCALIZED PARTIAL MASTECTOMY PROCEDURE, IT WAS NOTED BY THE SURGEON THAT THE PERFORATED END OF THE VIDEO DRAPE WAS SEPARATED. THIS CAUSED THE PROBE TO BE EXPOSED. THE PROCEDURE WAS EXTENDED DUE TO HAVING TO REESTABLISH STERILE FIELD AND RE-WRAP THE PROBE WITH DRAPE. STAFF HAVE STARTED RELOCATING THE PROBE END TO ANOTHER LOCATION AND SECURING WITH THE STERILE TAPE PROVIDED IN THE DRAPE KIT.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 19557214 ↗
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- Medline DYNJP2416Medline Industries, Inc. · Drape, surgical2 recalls1 report
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- Medline DYNJP2418Medline Industries, Inc. · Drape, surgical2 recalls0 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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