Skip to content

FABCO 34911510Recalls & reported problems

First Aid Bandage CO Inc · Class 1

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Aug 2, 2022Open, Classified

    Sterility with new cotton source not validated

    Z-1747-2022 · Root cause: Component change control · FDA record ↗

Other Dissector, Surgical, General & Plastic Surgery devices

All Dissector, Surgical, General & Plastic Surgery devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.