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. 2,642 recalls have been distributed to Texas in the last 12 months.
Showing 38681–38700 of 55,713 recalls
Recalled Item: Convenience Kits from Centurion that contain an In-Vision- Plus Needleless...
The Issue: Convenience Kits contain an In-Vision-Plus Needleless IV Connector, code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics Due to Software Issue
The Issue: Software Issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Naturalyte Liquid Acid Concentrate Catalog Number: 08-2301-3...
The Issue: On the label calcium (Ca) listed in the right upper corner of the label (red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile wDR motorized portable diagnostic X-ray systems. Intended for use...
The Issue: This is related to previous 806 Notifications about uncommanded movements of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A Picture Archiving and Communication System (PACS) intended to display...
The Issue: To inform users about the possible incorrect values for Distance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEA / CD66e Ab-2 Recalled by Lab Vision Corporation Due to Certain lots of...
The Issue: Certain lots of CEA/CD66e Ab2 were produced with a dilution factor of 1:100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclopentolate Hydrochloride Ophthalmic Solution USP Recalled by Bausch &...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...
The Issue: Labeling: label error on declared strength.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...
The Issue: Labeling: label error on declared strength.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Tablets USP Recalled by Amerisource Health Services Due to...
The Issue: Failed Dissolution Specifications: Unexplained low out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Licorice Coughing Liquid (guaifenesin) Recalled by Master Herbs, Inc./Li Due...
The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Jadak Barcode Scanner Recalled by CareFusion 303, Inc. Due to Customers...
The Issue: Customers reported issues when scanning medications with the scanners. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for...
The Issue: Reports where the Mylar/Tyvek pouch for RESTORIS MCK Baseplate in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.3mm Turbo-Power OTW Recalled by Spectranetics Corp. Due to The product is...
The Issue: The product is labeled with an expiration date that is past its shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OraQuick HCV Visual Panel Intended to assist new operation Recalled by...
The Issue: OraSure Technologies, Inc. discovered the package insert included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Battery Charger II (UBC II) Recalled by The Anspach Effort, Inc....
The Issue: The device is reported to enter safe mode and is no longer able to charge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.