International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

PLUM LifeCare 5000 Series and PLUM XL Familiy of Infusers

Model / Serial
PLUM LifeCare 5000 Series and PLUM XL Familiy of Infusers Plum LifeCare 5000List Number: 02507Plum XLList Number: 11555Plum XLMList Number: 11846Plum XLDList Number: 11859ARTG Number: 138109
Product Classification
General Hospital and Personal Use Devices
Manufacturer
Hospira Pty Limited
1 Event
- Recall of PLUM LifeCare 5000 Series and PLUM XL Familiy of Infusers

Communication Engine in Plum A+ and A+3 Infusion Pump

Model / Serial
Communication Engine in Plum A+ and A+3 Infusion Pump Plum A+Pump: 12391 & 20792Communication Engine Modules:20677 & 20791 (respectively)Plum A+3Pump: 20678Communication Engine Modules: 20678ARTG Number: 138109
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Communication Engine in Plum A+ and A+3 Infusion Pump

GemStar 7 Therapy Pump and GemStar Pain Management Pump (Phase 3 pumps)

Model / Serial
GemStar 7 Therapy Pump and GemStar Pain Management Pump (Phase 3 pumps)List Numbers: 13000 and 13150ARTG Number: 138109
Manufacturer
Hospira Pty Limited
1 Event
- Recall of GemStar 7 Therapy Pump and GemStar Pain Management Pump (Phase 3 pumps)

Receptal System Liners and Canisters

Model / Serial
Receptal System Liners and CanistersAll list numbers affected
Product Classification
General Hospital and Personal Use Devices
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Receptal System Liners and Canisters

Dimetapp Saline Nasal Drops for Infants

Model / Serial
Dimetapp Saline Nasal Drops for InfantsBatch numbers: 21320 & 21465ARTG Number: 167019
Manufacturer
Pfizer Australia Pty Ltd
1 Event
- Recall of Dimetapp Saline Nasal Drops for Infants

Sapphire Administration IV Set AP424 ( Patient Controlled Analgesia IV set for use with the Sapph...

Model / Serial
Sapphire Administration IV Set AP424 ( Patient Controlled Analgesia IV set for use with the Sapphire infusion pump)Catalogue Number: 611637201Product reference: 12003-000-0015List Number: 16372A9601Batch Numbers: 0167000814, 0167001414, 0167001514, 0167001914 and 0167002414ARTG Number: 200689
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Sapphire Administration IV Set AP424 ( Patient Controlled Analgesia IV set for use with the Sapphire infusion pump)

Sapphire Infusion Pump

Model / Serial
Sapphire Infusion PumpHospira List Number: 163113601/163123601Q Core Number (on pump): 15031-000-0001 /15032-000-0001ARTG Number: 201499
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Sapphire Infusion Pump

Plum 360 Infusion Pump, Software Version 15.01.XX.009 List number 30010-27

Model / Serial
Plum 360 Infusion Pump, Software Version 15.01.XX.009 List number 30010-27 All serial numbers affectedARTG Number: 234421
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Plum 360 Infusion Pump, Software Version 15.01.XX.009 List number 30010-27

Sapphire Multi-Therapy and Sapphire Epidural Pumps with software versions 11.00 and below

Model / Serial
Sapphire Multi-Therapy and Sapphire Epidural Pumps with software versions 11.00 and belowHospira List Numbers:163113601 and 163123601Q Core Number (on pump): 15031-000-0001 and 15032-000-0001ARTG Number: 201499
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Sapphire Multi-Therapy and Sapphire Epidural Pumps with software versions 11.00 and below

Plum 360 Infusion Pump, with software version 15.02

Model / Serial
Plum 360 Infusion Pump, with software version 15.02List Number: 30010ARTG Number: 234421
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Plum 360 Infusion Pump, with software version 15.02

Plum 360 Infusion Pump, software version 15.02

Model / Serial
Plum 360 Infusion Pump, software version 15.02List Number: 30010ARTG Number: 234421
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Plum 360 Infusion Pump, software version 15.02

Hospira Plum 360 Infusion System

Model / Serial
Hospira Plum 360 Infusion SystemList Number: 30010Multiple Serial NumbersARTG Number: 234421
Product Classification
General Hospital and Personal Use Devices
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Hospira Plum 360 Infusion System

Plum 360 Infusion System

Model / Serial
Plum 360 Infusion SystemSoftware version: 15.10.00.010List Number: 30010ARTG Number: 234421
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Plum 360 Infusion System

Hospira labelled MedNet Medication Management Suite – with Plum 360 Infusion System

Model / Serial
Hospira labelled MedNet Medication Management Suite – with Plum 360 Infusion SystemVersion 6.1List Number: 16037-75-01Version 6.21List Number: 16037-75-02ARTG Number: 262489 (Hospira Pty Limited - Infusion pump medication dosage application software)
Manufacturer
Hospira Pty Limited
1 Event
- Recall of Hospira labelled MedNet Medication Management Suite – with Plum 360 Infusion System

Infusion and transfusion, administration sets infusion pump set. Primary Plumset

Model / Serial
Manufacturer
Hospira Inc
1 Event
- Recall of Infusion and transfusion, administration sets infusion pump set. Primary Plumset

Infusion and transfusion, administration sets infusion pump set. Administration sets (infusion pu...

Model / Serial
Manufacturer
Hospira Inc
1 Event
- Recall of Infusion and transfusion, administration sets infusion pump set. Administration sets (infusion pump, intravenous & blood transfusion)

Sapphire Multi Therapy Pump with software Rev09Ver07

Model / Serial
Manufacturer
Hospira Inc
1 Event
- Recall of Sapphire Multi Therapy Pump with software Rev09Ver07

Infusion and transfusion, administration sets, filter. Lifeshield, latex-free, non-DEHP.

Model / Serial
Manufacturer
Hospira Inc.
1 Event
- Recall of Infusion and transfusion, administration sets, filter. Lifeshield, latex-free, non-DEHP.

PLUM LifeCare 5000 Series and PLUM XL Family of Infusers

Model / Serial
Manufacturer
Hospira Pty Limited
1 Event
- Recall of PLUM LifeCare 5000 Series and PLUM XL Family of Infusers

Gemstar Infusion System

Model / Serial
Product Classification
General Hospital and Personal Use Devices
Manufacturer
Hospira Inc
1 Event
- Recall of Gemstar Infusion System

LifeShield LATEX-FREE HemoSet 100ml Burette I.V. PlumSet, Nonvented, 105 inch

Model / Serial
Manufacturer
Hospira Inc.
1 Event
- Recall of LifeShield LATEX-FREE HemoSet 100ml Burette I.V. PlumSet, Nonvented, 105 inch

Plum A+ Infusion Pump/ Plum A+ Infusion Pump v11.3/ Plum A+3 Infusion Pump v11.3/ Plum A+3 with H...

Model / Serial
Manufacturer
Hospira
1 Event
- Recall of Plum A+ Infusion Pump/ Plum A+ Infusion Pump v11.3/ Plum A+3 Infusion Pump v11.3/ Plum A+3 with Hospira MedNet Software/ Plum A+ Driver / Plum A+ Hyperbaric infusion system

About this database

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

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

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.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)