Medline Industries, Inc. DYNJ908320ARecalls & reported problems
Medline Industries, Inc. · LR GYN ROBOTIC · 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 10195327074890), received between Aug 10, 2026 and Aug 10, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Frayed” (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
- Material Frayed1
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.
MalfunctionAug 10, 2026Material Frayed
It was reported that "I have never seen this before and have no clue what this is".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50195842 ↗
Other Gynecological laparoscopic kit devices
- Medline Industries, Inc. DYNJ44864SMedline Industries, Inc. · Gynecological laparoscopic kit4 recalls0 reports
- Medline Industries, Inc. DYNJ909398AMedline Industries, Inc. · Gynecological laparoscopic kit4 recalls0 reports
- Medline Industries, Inc. DYNJ38844NMedline Industries, Inc. · Gynecological laparoscopic kit4 recalls0 reports
- Medline Industries, Inc. DYNJ66298DMedline Industries, Inc. · Gynecological laparoscopic kit3 recalls1 report
- Medline Industries, Inc. DYNJ906926BMedline Industries, Inc. · Gynecological laparoscopic kit3 recalls0 reports
- Medline Industries, Inc. DYNJ49191BMedline Industries, Inc. · Gynecological laparoscopic kit3 recalls0 reports
- Medline Industries, Inc. DYNJ52564DMedline Industries, Inc. · Gynecological laparoscopic kit3 recalls0 reports
- Medline Industries, Inc. CDS920099SMedline Industries, Inc. · Gynecological laparoscopic kit3 recalls0 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