FDA Class II · Medical device · August 19, 2026
BOBBY Balloon Guide Catheter REF recall — MICROVENTION INC.
Due to an increase rate of balloon pinhole defects.
Official ID Z-2912-2026 · Official record ↗
MICROVENTION recalls
2 recent recalls on record for MICROVENTION in connected official government data as of September 7, 2026 at 6:00 AM UTC.
Models with recalls
All MICROVENTION recalls
FDA Class II · Medical device · May 20, 2026
LVIS Intraluminal Support Device recall — MICROVENTION INC.
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to …
Official ID Z-2200-2026 · Official record ↗
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.