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CARDINAL HEALTH SBA57MN00ARecalls & reported problems

Cardinal Health 200, LLC · CHH FACIAL PLASTICS PACK · Class 1

Data updated Oct 16, 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.

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 16, 2026.

Recalls naming this device

  1. Nov 8, 2024Open, Classified

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

    Z-0913-2025 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

Other Ear, nose, and throat surgical tray devices

All Ear, nose, and throat surgical tray devices →

Sources and updates

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