International safety notice

• Sutura VICRYL™ y sutura antibacteriana VICRYL™ Plus • Sutura PDS™ II y sutura antibacteriana PDS™ Plus • Sutura MONOCRYL™ y sutura antibacteriana MONOCRYL™ Plus • Sutura PDS™ II Y sutura antibacteriana PDS™ Plus Ver códigos de producto afectados en la nota de aviso de la empresa.

Spain / AEMPS · ESP · Jun 4, 2024

Key facts

Title • Sutura VICRYL™ y sutura antibacteriana VICRYL™ Plus • Sutura PDS™ II y sutura antibacteriana PDS™ Plus • Sutura MONOCRYL™ y sutura antibacteriana MONOCRYL™ Plus • Sutura PDS™ II Y sutura antibacteriana PDS™ Plus Ver códigos de producto afectados en la nota de aviso de la empresa.
Regulator Spain / AEMPS
Country ESP
Brand • Sutura VICRYL™ y sutura antibacteriana VICRYL™ Plus • Sutura PDS™ II y sutura antibacteriana PDS™ Plus • Sutura MONOCRYL™ y sutura antibacteriana MONOCRYL™ Plus • Sutura PDS™ II Y sutura antibacteriana PDS™ Plus Ver códigos de producto afectados en la nota de aviso de la empresa.
Manufacturer Johnson & Johnson International. Bélgica. Ethicon LLC. EEUU.
Models CBJCHBCAABAAFIAQ1WMYH2YQDLIWEDNZFH8BIEVNX4WE, 2364579_ATTACHMENT, 106124, Z9210H, PDP9109H, W9125H, 28022, PDP9333H, 28042, W9101H, 106125, 2024-284 and 6 more
Event type Safety Notice
Date Jun 4, 2024

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 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

Browse all International device safety notices