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. 2,003 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,003 in last 12 months

Showing 2776127780 of 55,713 recalls

DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Gold Series Ultra Enhanced Indo Recalled by World Organix,...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 25, 2018· Leica Microsystems, Inc.

Recalled Item: Leica M530 OHX Microscope System Supplied with 100 - 120 Vac. Recalled by...

The Issue: Recall is due to a design weakness of the power insert module.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT CLEARVUE isp Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: Certain NAUTILUS DELTA Port Kit product code / lot number combinations may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2018· DJO, LLC

Recalled Item: This is an accessory to Intelect Advanced Recalled by DJO, LLC Due to The...

The Issue: The device accessories were not labeled with appropriate latex warning.

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

Class II — Potential Health HazardOngoing
DrugJune 22, 2018· Akorn, Inc.

Recalled Item: Acetylcysteine for Injection 6 g/30 mL (200 mg/mL). Rx Only. Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 22, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q. angiography system. Model 10848280 Recalled by Siemens Medical...

The Issue: Potential hardware issue which may cause thermal effects and possible damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Smiths Medical ASD Inc.

Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial...

The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Smiths Medical ASD Inc.

Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial...

The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee System Spacer Block Alignment Tower Recalled by Zimmer...

The Issue: The PPK System Spacer Block Alignment Tower mating feature that mates with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Clarity Diagnostics Llc

Recalled Item: Clarity Urocheck 10SG Urinalysis Strips Recalled by Clarity Diagnostics Llc...

The Issue: Clarity Diagnostics LLC discovered specific lots of Clarity 10SG Strips are...

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

Class III — Low RiskOngoing
Medical DeviceJune 22, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product...

The Issue: Potential hardware issue which may cause thermal effects and possible damage...

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

Class II — Potential Health HazardOngoing
FoodJune 22, 2018· Prinova US LLC

Recalled Item: Amino Life brand Product - BCAA 2:1:1 Instant Sunflower 25 Recalled by...

The Issue: This recall has been identified due to the detection of cyclamates...

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

Class III — Low RiskOngoing
Refund
FoodJune 22, 2018· Prinova US LLC

Recalled Item: Prinova brand Product - MRI Amintoten Strawberry Powder 25 Kgs Recalled by...

The Issue: This recall has been identified due to the detection of cyclamates...

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

Class III — Low RiskOngoing
Refund
FoodJune 22, 2018· Prinova US LLC

Recalled Item: Amino Life brand Product - L-Leucine Instant Sunflower 25 Kgs Recalled by...

The Issue: This recall has been identified due to the detection of cyclamates...

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

Class III — Low RiskOngoing
Refund
FoodJune 22, 2018· Talking Rain Beverage Co Inc

Recalled Item: Sparkling ICE Cherry Limeade Naturally Flavored Sparking Water Recalled by...

The Issue: Sparkling ICE Cherry Limeade, 17 oz. bottles, is recalled after the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 22, 2018· Prinova US LLC

Recalled Item: Prinova brand Product - Reginator NV (41825) 25 Kgs Fiber Recalled by...

The Issue: This recall has been identified due to the detection of cyclamates...

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

Class III — Low RiskOngoing
Refund
FoodJune 21, 2018· Blue Bell Creameries, L.P.

Recalled Item: Blue Bell Ice Cream Recalled by Blue Bell Creameries, L.P. Due to Vanilla...

The Issue: Vanilla ice cream not labeled for individual sale was distributed to stores...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

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

Class II — Potential Health HazardOngoing