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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

559

Past Year

11

Class I (Serious)

11

Most Recent

Nov 2025

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 461–480 of 559 recalls

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 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.: Hypodermic Needle-Pro 5 ml Syringe, 21g x 1'' Needle C...

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 Dual-Axis Swivel Adapter Catalog Number: 525151

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 4-Way Stopcock Catalog Number: T1206

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.

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 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 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 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 Lo-Profile Tracheostomy Tube Decannulation Cap Ca...

Sterility of the device is compromised due to packaging defects

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

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 ULTRA-FLO 4 - Way Stopcock Catalog Number: T1209

Sterility of the device is compromised due to packaging defects

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

Smiths Medical ASD, Inc.: Thermovent 1200, Heat and Moisture Exchanger Catalog # 5...

Sterility of the device is compromised due to lack of package integrity

FDAJul 13, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: ThermovenT 600, Heat and Moisture Exchangers Catalog #...

Sterility of the device is compromised due to lack of package integrity

FDAJul 13, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex Thermovent T, Heat and Moisture Exchangers Catalo...

Sterility of the device is compromised due to lack of package integrity

FDAJul 13, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: 15674-20 SPINAL(DD) 22/24G W/DRUGS

Trays contain Hospira recalled 2ml drug ampuls of 5% Lidocaine Hydrochloride with 7.5% Dextrose Injection, (NDC 0074-4712-01, lot number 09-568-DK) Hospira, Inc. was recalling the 2ml drug vials of 5% Lidocaine Hydrochloride w/ 7.5% Dextrose lot number 09-568-DK). The drug is being recalled due to reports of particulate in the product.

FDAJul 2, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: A2957 SPINAL (SDD) W/DRUGS K516566

Trays contain Hospira recalled 2ml drug ampuls of 5% Lidocaine Hydrochloride with 7.5% Dextrose Injection, (NDC 0074-4712-01, lot number 09-568-DK) Hospira, Inc. was recalling the 2ml drug vials of 5% Lidocaine Hydrochloride w/ 7.5% Dextrose lot number 09-568-DK). The drug is being recalled due to reports of particulate in the product.

FDAJul 2, 2004Nationwide• Smiths Medical ASD, Inc.