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. 1,142 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,142 in last 12 months

Showing 14341–14360 of 55,713 recalls

DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: RIVASTIGMINE TRANSDERMAL SYSTEM Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Enoxaparin Sodium Injection Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: ALBUTEROL SULFATE HFA Inhalation Aerosol Recalled by CARDINAL HEALTHCARE Due...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: SPIRIVA HANDIHALER (tiotropium bromide inhalation powder) 18 mcg/Capsule...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: FIRST LANSOPRAZOLE PT 3MG/ML Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Triamterene and Hydrochlorothiazide Capsules Recalled by CARDINAL HEALTHCARE...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 25, 2022· Blaine Labs Inc

Recalled Item: REVITADERM WOUND CARE GEL Recalled by Blaine Labs Inc Due to Microbial...

The Issue: Microbial Contamination of Non-sterile Product; FDA analysis found the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 25, 2022· Quesos La Ricura, Ltd.

Recalled Item: Quesos La Ricura Mi Ranchito Fresh Cheese with Hot Peppers Recalled by...

The Issue: May contain elevated levels of coliform

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 25, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: meridian bioscience immunocard STAT! Rotavirus test Recalled by MEDLINE...

The Issue: The product was incorrectly shipped at room temperature rather than .

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2022· Respironics California, LLC

Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1138747 Recalled by...

The Issue: A limited number of ventilators were assembled with expired adhesive. If the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 24, 2022· Argon Medical Devices, Inc

Recalled Item: 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6" Recalled by...

The Issue: Guidewire included with two lots of Arterial Line Kits would not fit through...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2022· Volcano Corp

Recalled Item: IntraSight Mobile IVUS Systems Recalled by Volcano Corp Due to...

The Issue: Multi-Modality Touch Screen Modules (MM-TSM), which are bedside/secondary...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 24, 2022· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053617 Recalled by...

The Issue: A limited number of ventilators were assembled with expired adhesive. If the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 24, 2022· Matrix Medical Network

Recalled Item: Matrix Clinical Solution At-Home COVID-19 Test Recalled by Matrix Medical...

The Issue: Due to COVID-19 Test not being authorized for home sample collection.

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

Class II — Potential Health HazardOngoing
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Ephedrine Plus (Ephedrine HCl 25mg Recalled by Ultra Seal Corporation Due to...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: Multi-Symptom Cramp Relief (acetaminophen 325mg and Pamabrom 25mg) Recalled...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: ELECTROLYTE Supplement Tablets (calcium 5.2 mg Recalled by Ultra Seal...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: CETAFEN COUGH & COLD COUGH & COLD RELIEF (Acetaminophen 325 mg Recalled by...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: REMfresh Advanced Ion-Powered Melatonin (Melatonin 5 mg) Caplets Recalled by...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2022· Ultra Seal Corporation

Recalled Item: SINUS DECONGESTANT Nasal Decongestant (phenylephrine HCl 5mg) tablets...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund