Halyard 69606Recalls & reported problems
O&M Halyard, Inc. · HALYARD* Isolation Gown Non-AAMI Procedure Chemo, Universal · Class 2
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 10680651696066), received between Sep 18, 2019 and Sep 18, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Defective Device1
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.
MalfunctionSep 18, 2019Defective Device
HALYARD DISPOSABLE ISOLATION GOWNS HAVE HAD ARMS SEWN SHUT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9081563 ↗
Other GOWN, ISOLATION, SURGICAL devices
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- CARDINAL HEALTH AT6200-XLCardinal Health 200, LLC · Gown, isolation, surgical1 recall0 reports
- CARDINAL HEALTH AT6588-BDCardinal Health 200, LLC · Gown, isolation, surgical1 recall0 reports
- CARDINAL HEALTH AT6588-XLCardinal Health 200, LLC · Gown, isolation, surgical1 recall0 reports
- CARDINAL HEALTH AT6688-XLCardinal Health 200, LLC · Gown, isolation, surgical1 recall0 reports
- CARDINAL HEALTH AT6688-BDCardinal Health 200, LLC · Gown, isolation, surgical1 recall0 reports
- CARDINAL HEALTH AT6100-XLCardinal Health 200, LLC · Gown, isolation, surgical1 recall0 reports
- CARDINAL HEALTH AT6100Cardinal Health 200, LLC · Gown, isolation, surgical1 recall0 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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