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Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc. Recalls

All product recalls associated with Smiths Medical ASD, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

34

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 20441–20460 of 21319 recalls

Smiths Medical ASD, Inc.: Portex Single Swivel Adapter Catalog Number: 525451

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex Tracheostomy Tube Decannulation Cap for use only w...

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex High Pressure 4 - Way Stopcock Catalog Number: T8202

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

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Smiths Medical ASD, Inc.: Portex Pro-Vent Arterial Blood Sampling Kit with Dry Lith...

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex 1-Way Stopcock Catalog Number: T1201

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex Custom Pro-Vent Arterial Blood Sampling Kit Catal...

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex PEEP-KEEP Dual-Axis Swivel Adapter Catalog Numbe...

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex Hypodermic Needle-Pro 5 ml Syringe, 20g x 1 '' N...

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex 3 Way Stopcock Catalog Number: T1102

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex 4 Way ''T-Handle'' Stopcock Catalog Number: T1204

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex High Pressure 1 - Way Stopcock Catalog Number: T...

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex 4-Way Stopcock Catalog Number: T1206

Sterility of the device is compromised due to packaging defects

FDASep 9, 2004Nationwide• Smiths Medical ASD, Inc.

Toshiba American Med Sys Inc: X-Ray High Voltage Generator, Model KXO-80G used on Image...

Non-compliance with Radiation Standards. Incorrect display of the radiographic time, due to software anomaly.

FDASep 7, 2004Nationwide• Toshiba American Med Sys Inc

Stryker Howmedica Osteonics Corp.: Long Length Dyax Nail.

Stryker became aware that Catalog number 1594-1130S, Lot Code K559623 was manufactured with a lag screw hold angulation of 135 degrees rather than 130 degrees.

FDASep 7, 2004Nationwide• Stryker Howmedica Osteonics Corp.

Medical Industries America Inc: Aeroneb Go Micropump Nebulizer Featuring OnQ electronic m...

The nebulizer can either fail or provide a low flow (partial dose) of medication

FDASep 7, 2004Nationwide• Medical Industries America Inc

General Electric Med Systems LLC: Emission Computed Tomography System. Including Model num...

GE Healthcare received reports of intermittent low ejection fraction (EF) results for MUGA (multi-gated acquisitions) studies on Millennium VG systems. This issue can occasionally lead to distortions in the volume curve in some MUGA studies, and result in calculated EF values lower (never higher) than actual values. A low EF value could lead to a physician decision to stop needed treatment.

FDASep 3, 2004Nationwide• General Electric Med Systems LLC

Fisher Diagnostic, A Company of Fisher Scientific LLC: Pacific Hemostasis brand SickleScreen Sickling Hemoglobin...

Defective reaction vials from an in vitro diagnostic test kit may cause positive patient samples to be interpreted as false negatives.

FDASep 3, 2004Nationwide• Fisher Diagnostic, A Company of Fisher Scientific LLC

Medical Industries America Inc: RemRest Non-Invasive Continuous Positive Airway Pressure ...

Units could show an error code and stop functioning.

FDASep 3, 2004CO, FL, IL +9 more• Medical Industries America Inc

General Electric Med Systems LLC: LOGIQ 5 system models 2331752, 2331753, 2332750, 2353313...

The Estimated Fetal Weight (EFW) result will be incorrect if the operator fails to perform the 'end exam' or new patient registration step before starting an EFW measurement procedure on the next patient.

FDASep 2, 2004Nationwide• General Electric Med Systems LLC

Electric Scooters (Leoch) – Vehicle Safety Concern (2004)

The recall involves Leoch-brand scooters that were also sold under the names "E-Scooter" and "Red Dragon." The scooters have a seat, two wheels and footrests on each side. A sticker on the left footrest reads, "E-Scooter." On the right footrest there is a sticker with a horse-head image. A serial number is printed underneath the left footrest. The affected scooter's model number is DK24250-3.

CPSCSep 2, 2004Nationwide• Leoch E-Vehicle Ltd.