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. 1,941 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,941 in last 12 months

Showing 4052140540 of 55,713 recalls

DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL Citrate 1 MCG/mL in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Akorn, Inc.

Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn, Inc. Due to...

The Issue: Defective Container: Product missing safety seal around the neck of the...

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

Class III — Low RiskOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: HEParin Sodium 0.5 USP UNITS/mL in 0.225% SODIUM CHLORIDE Recalled by...

The Issue: Stability Data Does Not Support Expiry

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL citrate in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: Atropine Sulfate Injection Solution Recalled by Cantrell Drug Company Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL citrate in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: LIDocaine HCl 1% BUFFERED WITH SODIUM BICARBONATE Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator Recalled by...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL CITRATE 4 MCG/mL in 0.9% SODIUM CHLORIDE Injection Recalled by...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL Citrate 50 mcg/mL in Sterile Water for Injection Recalled by...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL CITRATE 25 mcg/mL in 5% DEXTROSE Injection Recalled by Cantrell...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution...

The Issue: Lack of Assurance of Sterility; potential exposure to non-sterile lubricant...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Silarx Pharmaceutical, Inc.

Recalled Item: Lamivudine Oral Solution Recalled by Silarx Pharmaceutical, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date - Firm received a...

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

Class III — Low RiskOngoing
Refund
DrugAugust 20, 2015· Hospira Inc.

Recalled Item: Ketamine Hydrochloride Injection Recalled by Hospira Inc. Due to Defective...

The Issue: Defective Container: There were customer complaints of cracked and leaking...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 20, 2015· Akorn, Inc.

Recalled Item: RIFAMPIN FOR INJECTION USP Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurity/Degradation Specifications: Out of Specifications result...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 20, 2015· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Aliquot Delivery Kit (Syringe and Plunger) Recalled by Orthovita, Inc., dBA...

The Issue: Two isolated instances of holes in the outer header bag component of the...

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

Class II — Potential Health HazardOngoing
FoodAugust 20, 2015· Chetak New York, LLC

Recalled Item: Deep All Natural Spices Coriander Powder Recalled by Chetak New York, LLC...

The Issue: Chetak New York L.L.C. of Edison, NJ is recalling 300 jars of 14.1oz Deep...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 19, 2015· Covidien LLC

Recalled Item: Physio-Control QuikCombo Pacing/Defibrillation/ECG Electrodes RediPak¿...

The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound System with software versions VB10B and lower...

The Issue: The ACUSON SC2000 ultrasound system considers uppercase/lowercase...

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

Class II — Potential Health HazardOngoing