International safety notice

Smith & Nephew recall the sterile wound dressing Opsite Post-Op

Germany / BfArM · DEU · Dec 8, 2005

Key facts

Title Smith & Nephew recall the sterile wound dressing Opsite Post-Op
Regulator Germany / BfArM
Country DEU
Brand Smith & Nephew recall the sterile wound dressing Opsite Post-Op
Manufacturer Smith & Nephew recall the sterile wound dressing Opsite Post-Op
Models LOHFELDZ1, 66000712, 70012, 34253, 30.06.2005, MAX-PTANCK-STR.1-3, 350125, 80080, 24.10.05
Date Dec 8, 2005
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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

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