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  • Device 636
  • Manufacturer 87
  • Event 124969
  • Implant 0
Name Parent Company Source
Hospira Inc. Pfizer HPRA
Hospira Inc. Pfizer USFDA
Hospira Inc. Pfizer SMPA
Hospira Inc. Pfizer RLMPH
Hospira Inc. Pfizer SATP
Hospira, Inc Pfizer DMA
Hospira, Inc. Pfizer MHM
Hospira, Inc. Pfizer USFDA
Hospira, Inc. Pfizer SMPA
Hospira Inc., A Pfizer Company Pfizer USFDA
Hospira Inc. || Hospira Costa Rica Ltd. Pfizer NIDFSINVIMA
HOSPIRA INC. (USA) Pfizer NOM
Hospira Limited HK Pfizer DH
Hospira Nordic Pfizer DMA
HOSPIRA PORDUTOS HOSPITALARES LTDA Pfizer ANVSANVISA
Hospira Produtos Hospitalares Ltda. Pfizer ANVSANVISA
Hospira Produtos Hospitalares Ltda.; Hospira Inc. Pfizer ANVSANVISA
Hospira Pty Limited Pfizer RLMPH
Hospira Pty Limited Pfizer DHTGA
Hospira Sligo Pfizer AEMPSVFOI
Hospira UK Pfizer MHRA
Hospira UK Limited Pfizer ORMPMDBP
Hospira UK Limited Pfizer VNSAWH
Hospira UK Limited Pfizer AEMPSVFOI
Hospira UK Limited Pfizer DMA
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About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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