Skip to content

basixCOMPAK™ 00884450544570Recalls & reported problems

Merit Medical Systems, Inc. · Class 2

All models of basixCOMPAK (34)

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. Dec 4, 2025Open, Classified

    Inflation device handle may detach from the syringe during procedure.

    Z-1123-2026 · Root cause: Process control · Recall details · FDA record ↗

Other Syringe, Balloon Inflation, Exempt devices

All Syringe, Balloon Inflation, Exempt devices →

Sources and updates

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