Micro Therapeutics, Inc. recalls

3 recalls.

• Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code:... recall (Micro Therapeutics, Inc.)
  Medical deviceClass IIReported October 7, 2026 · 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.
• Pipeline Flex Embolization Device with Shield Technology recall (Micro Therapeutics, Inc.)
  Medical deviceClass IIReported July 29, 2026 · 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...
• Pipeline Flex Embolization Device with Shield Technology recall (Micro Therapeutics, Inc.)
  Medical deviceClass IIReported July 29, 2026 · 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...