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  • Device 636
  • Manufacturer 87
  • Event 124969
  • Implant 0
Name Classification Manufacturer Risk Class Country Source
Device Recall Plum A Infusion Pump, Single Channel General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Device Recall LifeCare PCA 3 General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Device Recall Hospira General Hospital and Personal Use Devices Hospira Inc., A Pfizer Company 2 United States USFDA
Device Recall Plum 360 Infusion Pump General Hospital and Personal Use Devices Hospira Inc., A Pfizer Company 2 United States USFDA
Device Recall Plum A Infusion Pump General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Device Recall Plum A3 Infusion Pump with Hospira MedNet Software General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Device Recall Plum A Infusion Pump with Hospira MedNet Software General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Device Recall Angiographic Syringe Cardiovascular Devices Hospira Inc. 2 United States USFDA
Device Recall Angiographic Syringe Cardiovascular Devices Hospira Inc. 2 United States USFDA
Device Recall Angiographic Syringe Cardiovascular Devices Hospira Inc. 2 United States USFDA
Device Recall Angiographic Syringe Cardiovascular Devices Hospira Inc. 2 United States USFDA
Device Recall Catheterization Kits Cardiovascular Devices Hospira Inc. 2 United States USFDA
Device Recall LifeShield LatexFree HEMA Blood PlumSet General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Device Recall Hospira Latex Free Blood Secondary Set General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Device Recall LifeShield LatexFree Primary I.V. Set General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Device Recall Hospira Transpac IV Monitoring Kit General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
Device Recall LifeShield OmniFlow Primary I.V. Pump Set General Hospital and Personal Use Devices Hospira Inc. 2 United States USFDA
All "GemStarTM infusion pumps", catalog number 13000, 13100, 13150, 13086, 13087 Hospira Sligo Spain AEMPSVFOI
Disposable Hospira 1L system (container and bag) Hospira UK Limited Spain AEMPSVFOI
Venisystems blood equipment with CAIR clamp Hospira Inc Spain AEMPSVFOI
LifeShieldTM, Latex-Free, Non-DEHP, Primary PlumSetTM Hospira Inc Spain AEMPSVFOI
Plum A + Infusion Pumps Hospira Inc Spain AEMPSVFOI
"IV Plum-Set Administration Teams", all batches manufactured as of July 2007 by Hospira Inc, USA. See affected references in the Notice of the company. Hospira Inc Spain AEMPSVFOI
Covers (liner) and boats (canister) of the "Receptal System", manufactured by Hospira Inc, USA. See affected references in the Notice of Company Notice Hospira Inc Spain AEMPSVFOI
Certain references and batches of IV administration equipment for the Lifecare 5000 / XL pump Hospira Inc. Spain AEMPSVFOI
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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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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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