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Endoflip RFG-EF100Recalls & reported problems

Covidien LP · Endoflip system 1.0 refurbished · Class 2

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. May 13, 2026Open, Classified

    Due to products are incorrectly flagged as expired due to the system's 24-hour usage limit, rendering the product unavailable for clinical procedures.

    Z-2950-2026 · Root cause: Under Investigation by firm · FDA record ↗

Other SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL) devices

All SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL) devices →

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