Skip to content

Medline Industries, Inc. DYNJRA1739BRecalls & reported problems

Medline Industries, Inc. · FEMORAL BLOCK TRAY · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

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.

Recalls naming this device

  1. Apr 27, 2026Class IIOpen, Classified

    Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

    Z-2442-2026 · Root cause: Process control · Recall details · FDA record ↗

  2. Oct 16, 2024Class IIOpen, Classified

    The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.

    Z-0509-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other Spinal epidural anesthesia kit devices

All Spinal epidural anesthesia kit devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page