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Devices
Device Recall Portex
Model / Serial
Lot Numbers: 102518, K163468, K176555, K510385, K520203, K529939, K532723, K533729, K586882, K633942, K675421, K676747, K681955, K682698
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
4904 Glass L.O.R. Syringe
Manufacturer
Smiths Medical ASD, Inc.
1 Event
Recall of Device Recall Portex
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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
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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.
112 more
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