Devices

Device Recall Portex

Model / Serial
Lot 490694
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
Blue Line Ultra Tracheostomy Tube 8.00mm Inner Cannula || REF 100/858/080
Manufacturer
Smiths Medical ASD, Inc.
1 Event
- Recall of Device Recall Portex

Manufacturer

Smiths Medical ASD, Inc.

Manufacturer Address
Smiths Medical ASD, Inc., 10 Bowman Dr, Keene NH 03431-5043
Manufacturer Parent Company (2017)
Smiths Group Plc
Source
USFDA

117 devices with a similar name

Learn more about the data here

Device Recall Portex

Model / Serial
Lot Numbers: K516347, K520553, K522055
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
A2526-24 SPINAL (SHB) W/DRUGS
Manufacturer
Smiths Medical ASD, Inc.

Device Recall Portex

Model / Serial
Lot Number: K520552
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
A2527-27 SPINAL (SHB) W/DRUGS
Manufacturer
Smiths Medical ASD, Inc.

Device Recall Portex

Model / Serial
Lot Numbers: K515876, K520197, K522302
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
A2613 SPINAL(FL)W/DRUGS
Manufacturer
Smiths Medical ASD, Inc.

Device Recall Portex

Model / Serial
Lot Number: K516579
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
A2624-22/25 SPINAL (SDD) W/DRUGS
Manufacturer
Smiths Medical ASD, Inc.

Device Recall Portex

Model / Serial
Lot Number: K515869
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
A2654-24 SPINAL (FL) W/DRUGS
Manufacturer
Smiths Medical ASD, Inc.

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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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