Skip to content

Medline Industries, Inc. DYNJRA1860Recalls & reported problems

Medline Industries, Inc. · SPINAL BLOCK 25G WHTCRE 5S BU · 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 10, 2026Class IOpen, Classified

    Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

    Z-2234-2026 · Root cause: Component design/selection · Recall details · FDA record ↗

  2. Oct 9, 2024Class IIOpen, Classified

    Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.

    Z-0649-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other Nerve block tray devices

All Nerve block tray devices →

Sources and updates

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