International safety notice

Batch Recall for Screw-vent®/Blank Screwvent/Abutment Blanks, ELOS Medtech

Germany / BfArM · DEU · Sep 16, 2014

Key facts

Title Batch Recall for Screw-vent®/Blank Screwvent/Abutment Blanks, ELOS Medtech
Regulator Germany / BfArM
Country DEU
Brand Screw-vent®/Blank Screwvent/Abutment Blanks, ELOS Medtech
Manufacturer Batch Recall for Screw-vent®/Blank Screwvent/Abutment Blanks, ELOS Medtech
Models 93139, AB-ZSV3515150, AB-ZSV5515150, 93138, 93140, AB-ZSV4515150, DK-3330
Date Sep 16, 2014
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 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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