Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,894 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,894 in last 12 months

Showing 2624126260 of 29,298 recalls

Medical DeviceSeptember 24, 2013· Baxter Healthcare Corp.

Recalled Item: SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP...

The Issue: Baxter Healthcare Corporation is recalling the LCD display screen on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Volcano Corp

Recalled Item: Volcano s5i/s5ix/s5iz/CORE Intravascular Ultrasound Imaging and Pressure...

The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Volcano Corp

Recalled Item: Volcano s5/s5x/CORE Mobile Intravascular Ultrasound Imaging and Pressure...

The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 22g/25g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs 26g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Alere San Diego, Inc.

Recalled Item: Alere Triage¿ TOX Drug Screen Control 1 Product Generic Name: Recalled by...

The Issue: Alere San Diego, Inc. initiated a voluntary recall of Alere Triage TOX Drug...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs 22g Quincke (Without Introducer)...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Baylis Medical Corp *

Recalled Item: Baylis Medical TorFlex Transseptal Guiding Sheath Recalled by Baylis Medical...

The Issue: The TorFlex Transseptal Guiding Sheath Kits are being recalled due to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs  25g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Regional Anesthesia Tray with Drugs Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre Recalled by Smiths...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Volcano Corp

Recalled Item: ComboMap Intravascular Flow and Pressure System Recalled by Volcano Corp Due...

The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Aesculap, Inc.

Recalled Item: Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)...

The Issue: The trial insertion instrument may disassemble during use due to a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Medrad Inc dba Bayer R&I

Recalled Item: MEDRAD¿ Stellant CT Injector System with Certegra Workstation Recalled by...

The Issue: The root cause investigation showed that the under-volume hazard can occur...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Maquet Cardiovascular, LLC

Recalled Item: Ultima OPCAB System Recalled by Maquet Cardiovascular, LLC Due to MAQUET has...

The Issue: MAQUET has identified a potential issue with the ULTIMA OPCAB (part numbers...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Midmark Corp dba Progeny Inc

Recalled Item: The Vantage Digital Panoramic System delivers high-value features standard...

The Issue: An error was identified in the Real Time Controller (RTC) firmware versions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2013· Atossa Genetics, Inc.

Recalled Item: Brand: The ForeCYTE Breast Health Test Recalled by Atossa Genetics, Inc. Due...

The Issue: Atossa Genetics is recalling ForeCYTE Breast Health Test, Mammary Aspiration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing