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. 1,866 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,866 in last 12 months

Showing 4646146480 of 55,713 recalls

FoodJune 9, 2014· Naturex Inc.

Recalled Item: Echinacea Agustifolia PE 4& echinosides The product is in powder Recalled by...

The Issue: Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 8, 2014· Dole Packaged Foods, Llc

Recalled Item: Dole Garden Soup "Roasted Garlic Tomato Basil" Recalled by Dole Packaged...

The Issue: Dole Packaged Foods is recalling Dole Garden Soup Roasted Garlic Tomato...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJune 6, 2014· Green Smoothie Girl

Recalled Item: GreenSmoothieGirl TriOmega Superfood Recalled by Green Smoothie Girl Due to...

The Issue: The products contain Organic Sprouted Chia Powder that may be contaminated...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugJune 6, 2014· Hospira Inc.

Recalled Item: Heparin Sodium in 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2014· Estee Lauder Inc

Recalled Item: DENBLAN Anticavity Fluoride Toothpaste Recalled by Estee Lauder Inc Due to...

The Issue: Stability Data Does Not Support Expiry

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 6, 2014· AGFA Corp.

Recalled Item: AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 Recalled by...

The Issue: When liquid comes in contact with the DX-D 100 touch screen, the device may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2014· Becton Dickinson & Co.

Recalled Item: Columbia Agar with 5% Sheep Blood Columbia Agar with 5% Recalled by Becton...

The Issue: A low level of surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2014· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Qube Compact Monitor Recalled by Spacelabs Healthcare...

The Issue: Spacelabs Healthcare is recalling Qube Compact Monitor, Model 91390, due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2014· Becton Dickinson & Co.

Recalled Item: CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Recalled by Becton...

The Issue: A low level of surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2014· Hospira Inc.

Recalled Item: The Hospira MedNet Medication Management Suite (MMS). Product Usage: The...

The Issue: Hospira MedNet 5.5, 5.8.1, and 5.8.2 contains software defect where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2014· BD Biosciences, Systems & Reagents

Recalled Item: BD FACS Canto and associated Fluidics Cart Product Usage: Flow Recalled by...

The Issue: Laser cooling fans and internal fan of the associated fluidics cart are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips Medical System Allura Xper X-Ray Angiographic Recalled by Philips...

The Issue: In certain circumstances, a software error can lead to a situation where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2014· Becton Dickinson & Co.

Recalled Item: TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) // Recalled by Becton...

The Issue: A low level of surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Chronic Hemodialysis Catheter Standard Kit Recalled by Argon...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Peel Away Kit Recalled by Argon Medical Devices, Inc Due to...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Exchange Kit Model Numbers 32001524 (24 cm) Recalled by Argon...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis or Artis zee system Product Usage: Axiom Artis Recalled by...

The Issue: There is a potential problem with the AXIOM Artis or Artis zee system in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee and Artis zeego systems. x-ray Recalled by Siemens Medical...

The Issue: There is a potential problem with Artis zee and Artis zeego systems running...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Humidifier Adaptor 040 Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak SW/EAU Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing