Devices

Device Recall Stryker 550 mL AutoFuser PainPump

Model / Serial
Lots 08143756115 through 08171768725.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Canada.
Product Description
Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 4 mL/hr, 2 mL bolus, 60 minute bolus refill, 1 x 10.0 in. catheter, sterile, REF 0535-426-010.
Manufacturer
Stryker Instruments Div. of Stryker Corporation
1 Event
- Recall of Device Recall Stryker 550 mL AutoFuser PainPump

Manufacturer

Stryker Instruments Div. of Stryker Corporation

Manufacturer Address
Stryker Instruments Div. of Stryker Corporation, 4100 E. Milham Ave., Kalamazoo MI 49001
Manufacturer Parent Company (2017)
Stryker
Source
USFDA

16 devices with a similar name

Learn more about the data here

Device Recall Stryker 550 mL AutoFuser PainPump

Model / Serial
Lots 08136753321 through 09125932990.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Canada.
Product Description
Stryker 550 mL AutoFuser PainPump, single site continuous, 10 mL/hr, sterile, REF 0535-100-000.
Manufacturer
Stryker Instruments Div. of Stryker Corporation

Device Recall Stryker 550 mL AutoFuser PainPump

Model / Serial
Lots 08136753322 through 09124929601.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Canada.
Product Description
Stryker 550 mL AutoFuser PainPump, dual site continuous, 4 mL/hr, sterile, REF 0535-400-200.
Manufacturer
Stryker Instruments Div. of Stryker Corporation

Device Recall Stryker 550 mL AutoFuser PainPump

Model / Serial
Lots 08142756254 through 09125933719.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Canada.
Product Description
Stryker 550 mL AutoFuser PainPump, dual site continuous, 4 mL/hr, 2 x 10.0 in. catheters, sterile, REF 0535-400-210.
Manufacturer
Stryker Instruments Div. of Stryker Corporation

Device Recall Stryker 550 mL AutoFuser PainPump

Model / Serial
Lots 08137753560 through 09114928341.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Canada.
Product Description
Stryker 550 mL AutoFuser PainPump, dual site continuous, 4 mL/hr, 2 x 2.5 in. catheters, sterile, REF 0535-400-225.
Manufacturer
Stryker Instruments Div. of Stryker Corporation

Device Recall Stryker 550 mL AutoFuser PainPump

Model / Serial
Lots 08136753330 through 09114927978.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Canada.
Product Description
Stryker 550 mL AutoFuser PainPump, dual site continuous, 4 mL/hr, 2 x 5.0 in. catheters, sterile, REF 0535-400-250.
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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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.

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