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. 2,795 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,795 in last 12 months

Showing 1440114420 of 55,713 recalls

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
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: 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: 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: 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
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
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 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· 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· 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
DrugJanuary 21, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Proctofoam HC (hydrocortisone acetate 1% and pramoxine hydrochloride 1%)...

The Issue: cGMP deficiencies

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 21, 2022· Integra LifeSciences Corp.

Recalled Item: Codman Cranial Access Kits- indicated when a craniotomy is required Recalled...

The Issue: Incorrect extended expiration dates identified on the outer box label only,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2022· Integra LifeSciences Corp.

Recalled Item: Codman Cranial Access Kits- indicated when a craniotomy is required Recalled...

The Issue: Incorrect extended expiration dates identified on the outer box label only,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2022· NeuMoDx Molecular Inc

Recalled Item: NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip Recalled by NeuMoDx...

The Issue: A risk for product contamination was identified for the affected product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2022· Stryker Sustainability Solutions

Recalled Item: Recalled by Stryker Sustainability Solutions Due to Mislabeling

The Issue: Mislabeling; dual-bladder tourniquet cuffs are labeled as single-bladder...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Microgenics Corporation

Recalled Item: QMS Tacrolimus Immunoassay CALIBRATOR SET QMS TACROLIMUS CAL Recalled by...

The Issue: Due to QMS Tacrolimus Calibrator recovering between 82 to 94% of their...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· SIGHT DIAGNOSTICS LTD

Recalled Item: The Sight OLO device is a computer vision based platform Recalled by SIGHT...

The Issue: In instances where custom ranges were configured on the device post...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Ventana Medical Systems Inc

Recalled Item: BenchMark ULTRA and DISCOVERY ULTRA Instruments Recalled by Ventana Medical...

The Issue: Potential for Fluid Leak inside a staining system that could cause an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Outset Medical, Inc.

Recalled Item: Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000...

The Issue: Due to a component in the hemodialysis console there is the possibility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5 Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing