Devices

Device Recall Stryker PainPump

Model / Serial
Lot 2005060702.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide, Australia and Canada.
Product Description
Stryker PainPump1 Base Kit; Product number 500-100-000.
Manufacturer
Stryker Instruments Div. of Stryker Corporation
1 Event
- Recall of Device Recall Stryker PainPump

Manufacturer

Stryker Instruments Div. of Stryker Corporation

Manufacturer Address
Stryker Instruments Div. of Stryker Corporation, 4100 E Milham Ave, Portage MI 49002-9704
Manufacturer Parent Company (2017)
Stryker
Source
USFDA

69 devices with a similar name

Learn more about the data here

Device Recall Stryker PainPump

Model / Serial
Lot 2005060701.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide, Australia and Canada.
Product Description
Stryker PainPump1 5-Day Infusion Kit ; Product number 500-110-000.
Manufacturer
Stryker Instruments Div. of Stryker Corporation

Device Recall Stryker PainPump

Model / Serial
Lots 2005052002, 2005060703, 2005061401, 2005062001 and 2005063001.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide, Australia and Canada.
Product Description
Stryker PainPump1 2-Day Infusion Kit; Product number 500-120-000.
Manufacturer
Stryker Instruments Div. of Stryker Corporation

Device Recall Stryker PainPump

Model / Serial
Lot 2005051101 and 2005062301.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide, Australia and Canada.
Product Description
Stryker PainPump1 1-Day Infusion Kit; Product number 500-140-000.
Manufacturer
Stryker Instruments Div. of Stryker Corporation

Device Recall Stryker PainPump

Model / Serial
Lot 2005052501.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide, Australia and Canada.
Product Description
Stryker PainPump1 2-Site Y-Connector; Product number 500-200-000.
Manufacturer
Stryker Instruments Div. of Stryker Corporation

Device Recall Stryker PainPump

Model / Serial
Lot 2005053102.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide, Australia and Canada.
Product Description
Stryker PainPump1 2-Site Y-Connector; Product number 500-250-000.
Manufacturer
Stryker Instruments Div. of Stryker Corporation

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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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