Fresh Recalls

Micro Therapeutics recalls

3 recent recalls on record for Micro Therapeutics in connected official government data as of October 22, 2026 at 12:00 PM UTC.

Models with recalls

Pipeline Flex Embolization Device with Shield Technology (2)Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code (1)

All Micro Therapeutics recalls

FDA Class II · Medical device · October 7, 2026

Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code recall — Micro Therapeutics, Inc.

Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter.

Official ID Z-3326-2026 · Official record ↗

FDA Class II · Medical device · July 29, 2026

Pipeline Flex Embolization Device with Shield Technology recall — Micro Therapeutics, Inc.

Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm implants.

Official ID Z-2774-2026 · Official record ↗

FDA Class II · Medical device · July 29, 2026

Pipeline Flex Embolization Device with Shield Technology recall — Micro Therapeutics, Inc.

Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm implants.

Official ID Z-2773-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.