Medline Industries, Inc. DYND70288SRecalls & reported problems
Medline Industries, Inc. · SKN PREP SPNG STKS PVP PNT STR · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889942509850), received between Sep 8, 2026 and Sep 22, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Unsealed Device Packaging” (2 reports).
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
- Unsealed Device Packaging2
- Tear, Rip or Hole in Device Packaging1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Unsealed Device Packaging
It was reported that "The sterile pouch was open so the kit isn¿t sterile."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50853988 ↗MalfunctionSep 8, 2026Unsealed Device Packaging; Tear, Rip or Hole in Device Packaging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50671290 ↗
Other Skin prep tray devices
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- 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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