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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

257

Past Year

9

Class I (Serious)

0

Most Recent

Apr 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 181–200 of 257 recalls

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 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 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.

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Smiths Medical ASD, Inc.: Fiberoptic Bronchoscope Dual-Axis Swivel Adapter Catalog...

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.

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 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 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.: 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.: 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.: Smiths Medical ASD, Inc. Regional Anesthesia Trays contai...

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.

Smiths Medical ASD, Inc.: 4795-21 SADDLE BLOCK 25G QUINCKE 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.: A3075-25 SPINAL (SDD) 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.: A2152-25 SPINAL(FL)WHITACRE 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.: A2526-24 SPINAL (SHB) 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.: 49651-22 SPINAL 22G PENCIL POINT 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.: A2654-24 SPINAL (FL) 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.