International safety notice

Dispositivos de malla BARD para el prolapso del órgano pélvico y la incontinencia urinaria de esfuerzo de la mujer.

Spain / AEMPS · ESP · Mar 29, 2019

Key facts

Title Dispositivos de malla BARD para el prolapso del órgano pélvico y la incontinencia urinaria de esfuerzo de la mujer.
Regulator Spain / AEMPS
Country ESP
Brand Dispositivos de malla BARD para el prolapso del órgano pélvico y la incontinencia urinaria de esfuerzo de la mujer.
Manufacturer Bard Medical Division (BMD), Estados Unidos.
Models 35002, BRD805SI, BRD800SI, BRD301RS, 50855, BRD100R, 486201, 486101, BRD500HL, 2019-156, 57-61, 91.822.52.89 and 15 more
Event type Safety Notice
Date Mar 29, 2019

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