MicroVention Terumo Microplex 10 recall

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Catalog/lot numbers: 100515HC-R-V - 1903135RL, 1905135RL, 1903115LL, 1903135LL, 1903155LL, 1903225LL, 1904015LL, 1904175LL, 1905025LL, 1905035LL, 1905065LL, and 1905085LL; 100515HCSR-R-V - 1903225UL, 1904245UL, 1903045WL, 1903115WL, 1904015PL, 1904225WL, 1905065WL, and 1905225WL; 100520HC-R-V - 1905175LL, 1905205LL, 1905205VL; 100520HCSR-R-V - 1904245UL, 1904295UL, and 1903085WL; 100620HC-R-V - 1903115LL, 1905035LL, and 1905065LL; 100620HCSR-R-V - 1904245UL; 100730HC-R-V - 1905155LL, 1905175LL, and 1905225LL; 100730HCSR-R-V - 1904175PL, 1904225WL, and 1905035WL; 100830HC-R-V - 1905135RL, 1905135LL, and 1905175LL; 100930HC-R-V - 1903115LL; 100930HCSR-R-V - 1903085ZL, 1903115UL, 1903135UL, and 1904245UL; 101030HC-R-V - 1903135RL; and 101030HCSR-R-V - 1904245UL and 1903015RL.

Product

MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, Helical 10 Regular, Sterile, Rx, REF numbers 100515HC-R-V…

Recalling firm

Microvention, Inc.

Quantity

486 units

Distribution

All distribution was OUS. The countries receiving affected product are: Albania, Austria, Belarus, Belgium, Brazil, Bulgaria, China, Cyprus, Czech Republic, Denmark, Egypt, Finalnd, France, Georgia, Germany, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea, Latvia, Lebanon, Malta, Morocco, Netherlands, Norway, Poland, Portugal, Republic of Serbia, Romania, Russian Federation, Slovak Republic, Slovenia, South Africa, Spain, Sweden, Switzerland, Syria, Turkey, Ukraine, United Arab Emirates, and United Kingdom.

Recall date

March 4, 2020

Classification

Class II

Status

Terminated

Agency

FDA (device)