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CARDINAL HEALTH SNE15SNF15Recalls & reported problems

Cardinal Health 200, LLC · SOUTHDALE NEURO PACK 115614 · Class 1

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

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Quick summary

This Cardinal Health orthopedic tray kit has no adverse event reports that name its identifier. It is named in 1 open recall from November 2024 about possible endotoxin contamination in non-sterile surgical strips and patties included in Presource kits.

AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

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

1 FDA recall record name this device's identifier, 1 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. Nov 8, 2024Class IIOpen, Classified

    Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.

    Z-1134-2025 · Root cause: Material/Component Contamination · Recall details · FDA record ↗

Other Orthopedic tray devices

All Orthopedic tray devices →

Sources and updates

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