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. 1,870 recalls have been distributed to Texas in the last 12 months.
Showing 44261–44280 of 55,713 recalls
Recalled Item: Texamerican Cumin 5 lbs. Item Number: ARCH075-05 Recalled by Texamerican...
The Issue: Texamerican Food Blending received notification from its supplier that two...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Flavor Source Taco Seasoning 50 lbs. and 10 lbs. Item Recalled by...
The Issue: Texamerican Food Blending received notification from its supplier that two...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Texamerican Jalapeno Seasoning 50 lbs. Item Number: TF1422701 (R&D only)...
The Issue: Texamerican Food Blending received notification from its supplier that two...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Texamerican Glaze Mix 25 lbs. Item Number TF2710901 Recalled by Texamerican...
The Issue: Texamerican Food Blending received notification from its supplier that two...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Texamerican Chili Powder: 5 lbs. Item Number: ARCH064-50 Recalled by...
The Issue: Texamerican Food Blending received notification from its supplierthat two...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FERROUS SULFATE ELIXIR 220 mg/5 mL Recalled by Hi-Tech Pharmacal Co., Inc....
The Issue: Out-of-specification result for pH observed during stability testing of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benzonatate Capsules Recalled by Zydus Pharmaceuticals USA Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: The firm received a complaint of an embedded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Baxter Healthcare Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Complaints of leaks due to an incomplete...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shape-HF Cardiopulmonary Testing System Disposable Patient Interface (DPI)....
The Issue: This recall has been initiated because use of the impacted DPIs could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAR-Infrared Heat Home Sauna Recalled by Therasage, LLC. Due to Product...
The Issue: Product distributed without 510(k) approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portable FAR Infrared Sauna Indications including Recalled by Therasage,...
The Issue: Product distributed without 510(k) approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lubricated Intubating Stylet 6FR that is inserted into an endotracheal...
The Issue: A small piece of the stylet sheath has the potential to shear off upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAR-Infrared Heat Home Sauna Recalled by Therasage, LLC. Due to Product...
The Issue: Product distributed without 510(k) approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx monitor/defibrillator Models M3535A Recalled by Philips...
The Issue: MRx monitor/defibrillator could reboot at an indeterminate time, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flyte Togas are components of the Stryker Flyte System and Recalled by...
The Issue: A single lot (11121171) of Flyte Toga Peel-away X-Large (catalog number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses...
The Issue: One unit from a demo lot of POWERFLEX PRO PTA Dilatation Catheter was left...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mexican Chocolate ice cream Recalled by Full Tilt Ice Cream Due to Potential...
The Issue: Full Tilt Brand ice cream is being recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mudhoney ice cream Recalled by Full Tilt Ice Cream Due to Potential Listeria...
The Issue: Full Tilt Brand ice cream is being recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ube ice cream Recalled by Full Tilt Ice Cream Due to Potential Listeria...
The Issue: Full Tilt Brand ice cream is being recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.