Micro Therapeutics, Inc. recalls
3 recalls filed under Micro Therapeutics, Inc.. The most recent was published October 7, 2026.
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Class II · 18 days ago
Micro Therapeutics, Inc. Pipeline Flex Embolization Device with Shield Technology REF recall: Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm
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.
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Class II · 3 months ago
Micro Therapeutics, Inc. Pipeline Flex Embolization Device with Shield Technology recall: Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants
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…
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Class II · 3 months ago
Micro Therapeutics, Inc. Pipeline Flex Embolization Device with Shield Technology recall: Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants
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…
About this page
Micro Therapeutics, Inc. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.