International safety notice

Reactivo Access Hybritech p2PSA, referencia A49752.

Spain / AEMPS · ESP · May 26, 2023

Key facts

Title Reactivo Access Hybritech p2PSA, referencia A49752.
Regulator Spain / AEMPS
Country ESP
Brand Reactivo Access Hybritech p2PSA, referencia A49752.
Manufacturer Beckman Coulter, Inc. EE.UU.
Models 91.822.52.89, 41-43, LOTE234133, 2023-252, A49752, 234133, FA-23017, P2PSA, 94090, 08908, 20-40, 28108 and 2 more
Event type Safety Notice
Date May 26, 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

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