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. 1,049 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,049 in last 12 months

Showing 30201–30220 of 55,713 recalls

FoodSeptember 22, 2017· Silver Spring Foods, Inc.

Recalled Item: waterfront Bistro Tatar Sauce Recalled by Silver Spring Foods, Inc. Due to...

The Issue: Silver Spring is recalling Waterfront Bistro Tartar Sauce because an...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 22, 2017· Guangzhou Improve Medical Instruments Co., Ltd.

Recalled Item: Prevent G Safety Winged Blood Collection Set Glide - Rx Recalled by...

The Issue: Complain due to the hub needle came out when the nurse draw the blood and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Circulatory Technology Inc

Recalled Item: Better-Bladder cardiopulmonary bypass blood reservoir Recalled by...

The Issue: The device is used as part of extracorporeal membrane oxygenation (ECMO)...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier II in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Angiodynamics, Inc.

Recalled Item: Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015) Recalled by...

The Issue: Product was placed into distribution prior to completion of all required...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Circulatory Technology Inc

Recalled Item: **Recall Expanded to add these models: Bigger Better-Bladder cardiopulmonary...

The Issue: The device is used as part of extracorporeal membrane oxygenation (ECMO)...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier V in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier I in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier IV in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier III in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2017· Covidien LLC

Recalled Item: GastriSail" Gastric Positioning Device Product Usage: The GastriSail gastric...

The Issue: Reports of gastric or esophageal perforation occurring in procedures where...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2017· Medtronic Neuromodulation

Recalled Item: Medtronic Ascenda(R) Intrathecal Catheter Recalled by Medtronic...

The Issue: There is a possibility that specific lots of catheters that have recently...

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

Class III — Low RiskOngoing
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Catheter Insertion Kit Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Laceration Tray Recalled by Medline Industries Inc Due to Subpotent...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline General Purpose Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medical Equipment Affiliates IV Start Kit Recalled by Medline Industries Inc...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline General Purpose Kit Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray. Sterile. Single use only. Packaged in Recalled...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Skin Biopsy Pack-LF Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Skin Staple Remover Kit Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund