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. 2,858 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,858 in last 12 months

Showing 92819300 of 55,713 recalls

Medical DeviceJune 7, 2023· MICROVENTION INC.

Recalled Item: FRED Flow Re-Direction Endoluminal Device Recalled by MICROVENTION INC. Due...

The Issue: Intracranial aneurysm flow diverter device may be manufactured with an...

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

Class II — Potential Health HazardOngoing
DrugJune 6, 2023· HF Acquisition Co LLC

Recalled Item: GLYCOPYRROLATE INJECTION Recalled by HF Acquisition Co LLC Due to Labeling:...

The Issue: Labeling: Label Mix-up

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 6, 2023· Murata Vios, Inc.

Recalled Item: Vios Monitoring System Bedside Monitor Recalled by Murata Vios, Inc. Due to...

The Issue: A premature failure condition was identified with the L2050R pulse oximeter...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Implant Kit Recalled by...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...

The Issue: There is the potential for out of specification device geometries. widths,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2023· NeuroLogica Corporation

Recalled Item: OmniTom/OmniTom Elite- X-ray computed tomography applications for anatomy...

The Issue: 1. Wheels loosening over time with use of the device could lead to the...

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

Class II — Potential Health HazardOngoing
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Rinse Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: Arnica 7 Cream Recalled by Homeocare Laboratories, Inc. Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: SnoreStop Naso Spray Bulk Recalled by Homeocare Laboratories, Inc. Due to...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: Babelyn Diarrhea Drops Homeopathic Remedy Recalled by Homeocare...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Gel Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: Bebelyn Colic Drops Homeopathic Remedy Recalled by Homeocare Laboratories,...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Spray Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Rinse Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: DoloEar Earache Drops Recalled by Homeocare Laboratories, Inc. Due to cGMP...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund