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Devices
Device Recall Portex
Model / Serial
Lot Numbers; 102151, 103108, 103218, K132627, K148054, K156266, K163449, K176543, K197127, K211492, K535999, K555552, K586403, K626840, K667012, K678478, K705482
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
4902 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 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.
112 more
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