Medical DeviceOct 30, 2024
smiths medical portex, Nasopharyngeal Airway, Sizes as follows: a) AIRWAY NASOPHARYNGEAL recall — FDA Z-0143-2025
Uncertainty in the seal integrity of the sterile packaging.
Class IIFDA: OngoingSmiths Medical ASD Inc.
Recall history in this database
Classification mix: Class II: 119, Class I: 68, Class III: 6.
Medical DeviceOct 30, 2024
Smiths Medical ASD ENT RES, 100 ML, Non-Sterile W CLAMP & FEMALE LUER, Product Code recall — FDA Z-0018-2025
Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a…
Class IIFDA: OngoingSmiths Medical ASD Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TRANSTAR MONITORING KIT 1/EA, Product Code REF MX20103R1 recall — FDA Z-0185-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar DPT w/Stopcock & 30cc Flush 10/EA, Product Code REF recall — FDA Z-0194-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar KIDS KIT 7INCH CLOSED BLOOD SAMPLE KIT with 30cc/hr Flush recall — FDA Z-0200-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD ENT RES 100 ML Non-Sterile W CLAMP, TUBING FLAG, & FEMALE LUER, Product recall — FDA Z-0017-2025
Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a…
Class IIFDA: OngoingSmiths Medical ASD Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar KIDS KIT 34IN recall — FDA Z-0199-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar Patient Mount Monitoring Kit 10/EA, Product Code REF recall — FDA Z-0189-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar MONITORING SET W/SAMPLING PORT 10/EA, Product Code REF recall — FDA Z-0204-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar KIDS KIT 10IN recall — FDA Z-0201-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar DPT w/Two Stopcocks 10/EA, Product Code REF MX950X2SC recall — FDA Z-0195-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar 84in (213cm) Single Monitoring Kit 10/EA, Product Code REF recall — FDA Z-0192-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar 60in (152cm) Single Monitoring Kit 10/EA, Product Code REF recall — FDA Z-0191-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar SINGLE 84IN SET WITH ANTI-SHUNT STOPCOCK 10/EA, Product recall — FDA Z-0203-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code recall — FDA Z-0012-2025
Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a…
Class IIFDA: OngoingSmiths Medical ASD Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar Single ICP Set 1/EA, Product Code REF MX20897 recall — FDA Z-0183-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar Single OR Set 1/EA, Product Code REF MX20846R2 recall — FDA Z-0182-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar 72in (183cm) Double Monitoring Kit 10/EA, Product Code REF recall — FDA Z-0190-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar Neonatal Monitoring Kit 10/EA, Product Code REF MX9530T recall — FDA Z-0196-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar Kit w/ Stopcock1/EA, Product Code REF MX20740 recall — FDA Z-0186-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex NICU Monitoring Kit Set 1/EA, Product Code REF MX20086 recall — FDA Z-0184-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar KIDS KIT 19IN recall — FDA Z-0197-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar Disposable Transducer 1/EA, Product Code REF MX950 recall — FDA Z-0188-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar KIDS KIT 31IN recall — FDA Z-0198-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Smiths Medical Asd Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.