Medline Industries, Inc. DYKS1467Recalls & reported problems
Medline Industries, Inc. · PRE OP KIT · 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 10195327410193), received between Sep 14, 2026 and Sep 14, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (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.
Reports received per month
Most reported problems
Device problems
- Loss of or Failure to Bond1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 14, 2026Loss of or Failure to Bond
It was reported that the preop packs the Tegaderm tape is sticking to the wrong side of the paper.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50756167 ↗
Other Skin prep tray devices
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- Medline Industries, Inc. DYKS1128CMedline Industries, Inc. · Skin prep tray2 recalls0 reports
- MEDLINE INDUSTRIES, INC. DYKS1216IMedline Industries, Inc. · Skin prep tray2 recalls0 reports
- Medline Industries, Inc. DYNDL1643AMedline Industries, Inc. · Skin prep tray1 recall1 report
- MEDLINE INDUSTRIES, INC. DYKS1124CMedline Industries, Inc. · Skin prep tray1 recall0 reports
- Medline Industries, Inc. DYKS2018Medline Industries, Inc. · Skin prep tray1 recall0 reports
- Medline Industries, Inc. DYKS1043FMedline Industries, Inc. · Skin prep tray1 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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