Medline Industries, Inc. DYND70668Recalls & reported problems
Medline Industries, Inc. · SKIN PREP TRAY 4 COMPARTM TRAY · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10884389398425), received between Sep 1, 2026 and Sep 22, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Tear, Rip or Hole in Device Packaging” (6 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
- Tear, Rip or Hole in Device Packaging6
- Unsealed Device Packaging2
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Tear, Rip or Hole in Device Packaging
It was reported that "The perforation at the top of the bag makes it too easy to open and the OR is finding the bags open when they grab them from the supply cart. It appears the bags are opening during transit."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50859191 ↗MalfunctionSep 18, 2026Unsealed Device Packaging; Tear, Rip or Hole in Device Packaging
It was reported that product arrived with open packaging.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50818525 ↗MalfunctionSep 10, 2026Tear, Rip or Hole in Device Packaging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50721383 ↗MalfunctionSep 8, 2026Tear, Rip or Hole in Device Packaging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676440 ↗MalfunctionSep 8, 2026Tear, Rip or Hole in Device Packaging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50672007 ↗MalfunctionSep 1, 2026Unsealed Device Packaging; Tear, Rip or Hole in Device Packaging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50549593 ↗
Other Skin prep tray devices
- Medline Industries, Inc. DYKS1325AMedline Industries, Inc. · Skin prep tray2 recalls0 reports
- Medline Industries, Inc. DYKS1584AMedline Industries, Inc. · Skin prep tray2 recalls0 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page