International safety notice

- Catéter guiado para embolectomía TufTex®. Modelos 1651‐34, 1651‐38, 1651‐44, 1651‐48, 1651‐64, 1651‐68, 1651‐78,1651‐84, 1651‐88. ‐ Catéter para irrigación‐oclusión Pruitt®: 2102‐09. ‐ Catéter para Oclusión Pruitt®: 2103‐36, 2103‐46, 2103‐56.

Spain / AEMPS · ESP · May 21, 2025

Key facts

Title - Catéter guiado para embolectomía TufTex®. Modelos 1651‐34, 1651‐38, 1651‐44, 1651‐48, 1651‐64, 1651‐68, 1651‐78,1651‐84, 1651‐88. ‐ Catéter para irrigación‐oclusión Pruitt®: 2102‐09. ‐ Catéter para Oclusión Pruitt®: 2103‐36, 2103‐46, 2103‐56.
Regulator Spain / AEMPS
Country ESP
Brand - Catéter guiado para embolectomía TufTex®. Modelos 1651‐34, 1651‐38, 1651‐44, 1651‐48, 1651‐64, 1651‐68, 1651‐78,1651‐84, 1651‐88. ‐ Catéter para irrigación‐oclusión Pruitt®: 2102‐09. ‐ Catéter para Oclusión Pruitt®: 2103‐36, 2103‐46, 2103‐56.
Manufacturer LeMaitre Vascular Inc., EE.UU.
Models 1651‐64, 1651‐48, 1651‐88, 1651‐84, 1651‐68, 2102‐09, 1651‐34, 1651‐38, 2103‐36, 2103‐46, 1651‐78, 2103‐56 and 1 more
Event type Safety Notice
Date May 21, 2025

At a glance

  • No Recall
  • Yes Field safety notice

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

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