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StabiliT TOUCH™ Syringe 00884450662144Recalls & reported problems

Merit Medical Systems, Inc. · 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.

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. Aug 19, 2024Class IIOpen, Classified

    Inflation devices may have a small hole in the sterile barrier of the device and use of affected devices may result in exposure to pathogens/pyrogens which could lead to infection.

    Z-0073-2025 · Root cause: Packaging process control · Recall details · FDA record ↗

Other Injector, vertebroplasty (does not contain cement) devices

All Injector, vertebroplasty (does not contain cement) devices →

Sources and updates

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