Product Recalls in Texas

Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,723 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,723 in last 12 months

Showing 1796117980 of 30,921 recalls

Medical DeviceNovember 15, 2017· Cordis Corporation

Recalled Item: Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated...

The Issue: Potential for cracked luer hubs

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Alere San Diego, Inc.

Recalled Item: Triage Drugs of Abuse Plus TCA 25 Test Kit Recalled by Alere San Diego, Inc....

The Issue: The recalled lots have demonstrated unexpected false positive THC results.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath Recalled by...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen CVC Kit Recalled by Arrow International Inc...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump 3500 Series The Medfusion¿ Syringe Infusion Pumps...

The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Amendia, Inc dba Spinal Elements

Recalled Item: Piranha Screw 4.0 x 12mm Recalled by Amendia, Inc dba Spinal Elements Due to...

The Issue: Potential incorrect marking and color identification of Piranha screw. Some...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump 3010 Series The Medfusion¿ Syringe Infusion Pumps...

The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump 4000 Series The Medfusion¿ Syringe Infusion Pumps...

The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Cyberonics, Inc

Recalled Item: VNS Therapy Programmer Recalled by Cyberonics, Inc Due to Certain Model 3000...

The Issue: Certain Model 3000 programming events can result in miscalculation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· C.R. Bard, Inc.

Recalled Item: CritiCore Automated Urine Output and Temperature Monitor Recalled by C.R....

The Issue: Issues identified with the monitor including urine output measurement...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing