Medline DYNJ05156LFRecalls & reported problems
Medline Industries, Inc. · BNDG,ELSTC,MATRIX,STRL,6"X5YD,LF,HOOK&LP · Class 1
Data updated Oct 16, 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 10080196823529), received between Sep 22, 2026 and Sep 22, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination” (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
- Contamination1
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 22, 2026Contamination
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50854135 ↗
Other BANDAGE, ELASTIC devices
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- Surgitube® 220Derma Sciences Canada Inc · BANDAGE, ELASTIC1 recall0 reports
- Surgitube® 219Derma Sciences Canada Inc · BANDAGE, ELASTIC1 recall0 reports
- Surgitube® 242Derma Sciences Canada Inc · BANDAGE, ELASTIC1 recall0 reports
- Surgitube® 222Derma Sciences Canada Inc · BANDAGE, ELASTIC1 recall0 reports
- Surgitube® 243Derma Sciences Canada Inc · BANDAGE, ELASTIC1 recall0 reports
- PROFORE KIT LATEX FREE 66020626Smith & Nephew Medical Limited · Bandage, Elastic45 reports
- PROFORE 18-25CM ANKLE CIRC. Case 8 66000016Smith & Nephew Medical Limited · Bandage, Elastic19 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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