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. 2,697 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,697 in last 12 months

Showing 2108121100 of 30,921 recalls

Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass RX Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G Recalled by Becton...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2016· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod Recalled by...

The Issue: RTI Surgical Inc. (RTI) is conducting a voluntary recall on two specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· GE Healthcare, LLC

Recalled Item: Brivo XR385 Recalled by GE Healthcare, LLC Due to The placing of weight on...

The Issue: The placing of weight on the VRAD detector, of the Brivo XR385 digital...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Chemistry 1 Calibrator The Chemistry 1 Calibrator (KC110B)...

The Issue: Siemens determined that discrepant low calcium recovery of QC and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2016· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse PACS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...

The Issue: Image data for a patients image may not be correct

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2016· Keystone Dental Inc

Recalled Item: Keystone Dental PrimaConnex¿ Straight Implant TC Recalled by Keystone Dental...

The Issue: Small diameter (SD) cover screw was packaged with the regular diameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2016· Hand Biomechanics Lab Inc

Recalled Item: Agee-WristJack¿ Fracture Reduction System Recalled by Hand Biomechanics Lab...

The Issue: A number of Agee WristJack¿ Fracture Reduction Systems have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2016· Tearscience, Inc

Recalled Item: LipiFlow thermal Pulsation System Recalled by Tearscience, Inc Due to...

The Issue: Complaints related to an error condition occurring during patient treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2016· TEM Systems Inc

Recalled Item: ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US...

The Issue: Customers complained of low/empty reagent vials.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2016· A & D Enginering Inc

Recalled Item: Blood Pressure Monitor UA-767PBT-Ci for small cuff. Designed to be Recalled...

The Issue: A&D may have shipped blood pressure monitors that were not labeled for use...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Teleflex Medical

Recalled Item: Teleflex Percuaneous Solutions Recalled by Teleflex Medical Due to The...

The Issue: The product is being recalled due to a labeling error. The Gripper Graspers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Contour Fabricators Inc

Recalled Item: Zero-Gravity Radiation Protection System Radiology Personnel protective...

The Issue: Two customer complaints suggest that excessive rotation of the cable in one...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Teleflex Medical

Recalled Item: Teleflex Percuaneous Solutions Recalled by Teleflex Medical Due to The...

The Issue: The product is being recalled due to a labeling error. The Gripper Graspers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2016· Greatbatch Medical

Recalled Item: Greatbatch Stiffer Coaxial Micro-Introducer. Model #/ Name: 10904-001...

The Issue: Greatbatch Medical has identified an issue with the Stiffer Coaxial...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Celerity ECG Cable Accessory Pack Recalled by Angiodynamics Inc. (Navilyst...

The Issue: The Celerity ECG Cable Accessory Pack has the potential to contain an ECG...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2016· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation System (Product Code ENGEN) configured with...

The Issue: Ortho confirmed that it is possible for the mis-association of sample...

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

Class II — Potential Health HazardOngoing