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Bridge™ Prep Kit 00884450816509Recalls & reported problems

Merit Medical Systems, Inc. · Class 2

All models of Bridge Prep Kit (4)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

2 open recalls name 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
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 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. Apr 2, 2026Open, Classified

    catheter may experience resistance when being advanced over the guidewire

    Z-2003-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

  2. Jun 11, 2024Open, Classified

    Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

    Z-2567-2024 · Root cause: No Marketing Application · Recall details · FDA record ↗

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Sources and updates

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