Devices

Portex

Model / Serial
Lot numbers starting with: 0, 1, K1, K2, K51
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
Portex ULTRA-FLO 4 - Way Stopcock || Catalog Number: T1209
Manufacturer
Smiths Medical ASD, Inc.
1 Event
- Recall of 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

229 devices with a similar name

Learn more about the data here

Device Recall Portex

Model / Serial
Lot Number: K516574
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
15816-21 SPINAL(DD) 27G QUINCKE W/DRUGS
Manufacturer
Smiths Medical ASD, Inc.

Device Recall Portex

Model / Serial
Lot Number: K516550
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
15830-21 SPINAL(DD) 25G WHITACRE W/DRUGS
Manufacturer
Smiths Medical ASD, Inc.

Device Recall Portex

Model / Serial
Lot Number: K521691
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
15848-20 SPINAL(DD) 24G SPROTTE W/DRUGS
Manufacturer
Smiths Medical ASD, Inc.

Device Recall Portex

Model / Serial
Lot Numbers: K518603, K520640, K522835
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
15876-20 SPINAL(DD) 25G WHITACRE W/DRUGS
Manufacturer
Smiths Medical ASD, Inc.

Device Recall Portex

Model / Serial
Lot Number: K516575
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
15955-21 SPINAL(DD) 25G WHITACRE 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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