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. 2,905 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,905 in last 12 months

Showing 13611380 of 13,609 recalls

DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Dry Eye Relief (Polyethylene Glycol 400 Recalled by Cardinal...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5% Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Polyvinyl Alcohol 1.4% Lubricating Eye Drops Recalled by The Harvard Drug...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Dry Eye Relief (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Propylene Glycol Recalled by Cardinal...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lubricating Tears Eye Drops (Dextran/Hypromellose) Recalled by The Harvard...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 27, 2023· NCS Healthcare of Kentucky Inc

Recalled Item: Lisinopril Tablets USP 20 mg Recalled by NCS Healthcare of Kentucky Inc Due...

The Issue: Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine...

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

Class III — Low RiskOngoing
Refund
DrugOctober 27, 2023· NCS Healthcare of Kentucky Inc

Recalled Item: Buspirone Hydrochloride Tabs USP 10 mg Recalled by NCS Healthcare of...

The Issue: Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine...

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

Class III — Low RiskOngoing
Refund
DrugOctober 27, 2023· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Extended Phenytoin Sodium Capsules Recalled by Amneal Pharmaceuticals of New...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2023· VistaPharm LLC

Recalled Item: Mycophenolate Mofetil for Oral Suspension Recalled by VistaPharm LLC Due to...

The Issue: Defective Container: The adaptor does not fit into the neck of the bottle...

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

Class III — Low RiskOngoing
Refund
DrugOctober 23, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Phenytoin Oral Suspension Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed Content Uniformity Specifications

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 23, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by Glenmark...

The Issue: Failed Impurities/Degradation Specifications:Out of Specification result...

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

Class III — Low RiskOngoing
Refund
DrugOctober 23, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Ranolazine Extended-Release Tablets 500mg Recalled by Glenmark...

The Issue: Failed Dissolution Specifications: Out of specification for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2023· Botanical Be

Recalled Item: Artri King con Origa y Omega 3 tablets Recalled by Botanical Be Due to...

The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled by Glenmark...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugOctober 20, 2023· Botanical Be

Recalled Item: Reumo Flex caplets Recalled by Botanical Be Due to Undeclared Diclofenac

The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2023· Botanical Be

Recalled Item: Kuka Flex Forte caplets Recalled by Botanical Be Due to Undeclared Diclofenac

The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Deferasirox Tablets for Oral Suspension Recalled by Glenmark Pharmaceuticals...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund