Medline Industries, Inc. PAIN1781Recalls & reported problems

Medline Industries, Inc. · CSE TRAY 17G/27G · 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 10195327043360), received between Apr 21, 2026 and Apr 21, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Complete Blockage” (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

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Complete Blockage1

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.

MalfunctionApr 21, 2026Complete Blockage
UNABLE TO FLUSH EPIDURAL CATHETER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24939133 ↗

Device details

UDI-DI	`10195327043360`
Brand	Medline Industries, Inc.
Model	PAIN1781
Company	Medline Industries, Inc.
Product code	OFT · Spinal epidural anesthesia kit
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jul 28, 2023

Device type (GMDN): General surgical procedure kit, medicated

A typically non-dedicated collection of various surgical instruments, sometimes with dressings and/or other materials, and that includes a pharmaceutical component, intended to be used during: 1) open abdominal surgery; 2) a range of open surgical procedures across multiple clinical specialties (non-dedicated); 3) non-orthopaedic trauma surgery; 4) minor dermatological surgery; or 5) cosmetic surgery below the head. As a kit that includes procedural devices, it is neither dedicated to surgical scrubbing, surgical patient preparation, nor anaesthesia, and is not a dedicated biopsy kit. This is a single-use device.

Other Spinal epidural anesthesia kit devices

Medline Industries, Inc. DYNJRA9040
Medline Industries, Inc. · Spinal epidural anesthesia kit
2 recalls2 reports
Medline Industries, Inc. DYNJ34418M
Medline Industries, Inc. · Spinal epidural anesthesia kit
2 recalls1 report
Design Options® 530184
B. Braun Medical Inc. · Spinal epidural anesthesia kit
2 recalls1 report
Design Options® 530159
B. Braun Medical Inc. · Spinal epidural anesthesia kit
2 recalls0 reports
Medline Industries, Inc. DYNJ34418L
Medline Industries, Inc. · Spinal epidural anesthesia kit
2 recalls0 reports
Medline Industries, Inc. DYNJRA1849
Medline Industries, Inc. · Spinal epidural anesthesia kit
2 recalls0 reports
Medline Industries, Inc. DYNJRA1739B
Medline Industries, Inc. · Spinal epidural anesthesia kit
2 recalls0 reports
Medline Industries, Inc. DYNJRA1739A
Medline Industries, Inc. · Spinal epidural anesthesia kit
2 recalls0 reports

All Spinal epidural anesthesia kit devices →

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