Medline Industries, Inc. DYNJRA1665BRecalls & reported problems
Medline Industries, Inc. · PAIN TOWEL TRAY · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10195327571061), received between Jun 10, 2024 and Nov 25, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Contamination” (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
- Contamination2
- Device Contamination with Chemical or Other Material1
- Particulates1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 25, 2025Contamination; Contamination
ACCORDING TO THE FACILITY, WHILE MEDICATION WAS BEING DRAWN UP INTO THE SYRINGE, IT WAS NOTED THAT THERE WAS A "BLACK FOREIGN OBJECT IN SYRINGE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23649015 ↗MalfunctionNov 25, 2025Contamination; Contamination
IT WAS REPORTED THAT ON (B)(6) 2025, A BLACK FOREIGN OBJECT WAS FOUND WITHIN THE SYRINGE WHILE MEDICATION WAS BEING DRAWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23645471 ↗MalfunctionNov 25, 2025Particulates; Particulates
A BLACK FOREIGN OBJECT WAS OBSERVED INSIDE THE SYRINGE WHILE DRAWING UP MEDICATION. THIS CAUSED A MINOR PROCEDURAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23643677 ↗MalfunctionJun 10, 2024Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED ON 05/13/2024 AFTER DRAWING UP "KENALOG" THERE WAS A PARTICULATE NOTED TO BE LOCATED "INSIDE THE SYRINGE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19505472 ↗
Other Spinal epidural anesthesia kit devices
- Medline Industries, Inc. DYNJRA9040Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls2 reports
- Medline Industries, Inc. DYNJ34418MMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls1 report
- Design Options® 530184B. Braun Medical Inc. · Spinal epidural anesthesia kit2 recalls1 report
- Design Options® 530159B. Braun Medical Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJ34418LMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1849Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1739BMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1739AMedline Industries, Inc. · Spinal epidural anesthesia kit2 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