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. 2,768 recalls have been distributed to Texas in the last 12 months.
Showing 17301–17320 of 55,713 recalls
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO156Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL494...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO180Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL476...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System Tray Sysem knee implant devices as follows: Recalled by...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL488...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL482...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential issue on the Revolution CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer - Product Usage: intended to assist in the...
The Issue: When the Cross Enterprise Display option is enabled on the Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS...
The Issue: Siemens has become aware of a potential issue with software version VE20C....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protek Solo Venous Dilator Set: dilator Recalled by Cardiac Assist, Inc Due...
The Issue: On 02/26/2021, it was found that there were incorrectly packaged Dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte...
The Issue: Users may observe additional locus specific signals at 9q34. The device pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum IQ - Infusion Pump - Product Usage: intended to Recalled by Baxter...
The Issue: Potentially defective component in the AC power adapter which may fail over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sp-4 Recalled by Washington Homeopathic Products, Inc. Due to An error...
The Issue: An error occurred where the product was manufactured with Potassium Chloride...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LCL-2-0191 Recalled by Washington Homeopathic Products, Inc. Due to An error...
The Issue: An error occurred where the product was manufactured with Potassium Chloride...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Macula Pellets Homeopathic Medicine Recalled by Washington Homeopathic...
The Issue: An error occurred where the product was manufactured with Potassium Chloride...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.