International safety notice

Immucor Medizinische Diagnostik GmbH. Robert-Bosch-Str. 32 63303 Dreieich, Alemania.

Spain / AEMPS · ESP · May 10, 2023

Key facts

Title Immucor Medizinische Diagnostik GmbH. Robert-Bosch-Str. 32 63303 Dreieich, Alemania.
Regulator Spain / AEMPS
Country ESP
Brand Immucor Medizinische Diagnostik GmbH. Robert-Bosch-Str. 32 63303 Dreieich, Alemania.
Manufacturer Immucor, Inc., EEUU.
Models 10222234001256, 0066240, 30071, 8056-100, 93084, 2023-226, 26520, 80560, LOTE226520, 855.466.8267, 91.822.52.89, 226520 and 3 more
Event type Safety Notice
Date May 10, 2023

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