International safety notice

Sistema láser de Philips, referencia LAS-100, fabricados antes del 18 de mayo de 2022.

Spain / AEMPS · ESP · Jun 17, 2022

Key facts

Title Sistema láser de Philips , referencia LAS-100, fabricados antes del 18 de mayo de 2022.
Regulator Spain / AEMPS
Country ESP
Brand Sistema láser de Philips , referencia LAS-100, fabricados antes del 18 de mayo de 2022.
Manufacturer Spectranetics Corp., EE.UU.
Models 2022-IGT-IGTD-002, CVX-300, 31202046550, 2022C02, 31202046555, 3222566604, 4722971709, 2022-305, 100104, JUN-2022, LAS-100, 80858 and 13 more
Event type Safety Notice
Date Jun 17, 2022

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 Matching catalog numbers in FDA data

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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