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. 2,680 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,680 in last 12 months

Showing 2634126360 of 55,713 recalls

DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Skin Irritation & Itch Response Homeopathic Formula Recalled by Beaumont...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Sore Throat & Laryngitis Response Homeopathic Formula Recalled by Beaumont...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Mitek Screw and Washer Depth Gauge Recalled by DePuy Mitek, Inc., a Johnson...

The Issue: The device has an offset in the design that results in a reading...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray BeneVision Distributed Monitoring System (DMS) Recalled by Mindray...

The Issue: The firm has identified performance anomalies with the device caused when...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Arrow International Inc

Recalled Item: Arrow AGB + Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...

The Issue: The product was shipped after its expiry date due to a system error. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...

The Issue: Software anomalies were reported to affect the following system...

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

Class II — Potential Health HazardOngoing
FoodAugust 29, 2018· Cedarlane Natural Foods Inc/Frankly Fresh Foods Inc.

Recalled Item: CedarLane Organic Salads Recalled by Cedarlane Natural Foods Inc/Frankly...

The Issue: Discovery that the product is labeled as gluten free but contains wheat...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 28, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo 220/240V AC Recalled by Terumo Cardiovascular Systems Corporation Due...

The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Alcon Research, LTD.

Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...

The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2018· Alcon Research, LTD.

Recalled Item: CyPass ULTRA SYSTEM Recalled by Alcon Research, LTD. Due to Analysis of the...

The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2018· Hitachi Healthcare Americas Corp Informatics Division

Recalled Item: VidiStar(TM) PACS & DICOM Viewer Software system Recalled by Hitachi...

The Issue: The secure filesystem client software used in the interface between the...

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

Class II — Potential Health HazardOngoing