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. 1,866 recalls have been distributed to Texas in the last 12 months.
Showing 48401–48420 of 55,713 recalls
Recalled Item: Pumpkin Pie Fudge Recalled by Pecan Shed Due to Undeclared Allergens
The Issue: Presence of undeclared allergens soy, and milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dark Chocolate with Pecans Fudge Recalled by Pecan Shed Due to Undeclared...
The Issue: Presence of undeclared allergens soy, milk, and pecans
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Birthday Cake Fudge Recalled by Pecan Shed Due to Undeclared Allergens
The Issue: Presence of undeclared allergens soy & milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Liquid Mouse Monoclonal Antibody CD15 (NCL-L-CD15) Recalled by Leica...
The Issue: Product does not function as intended up to the expiry date on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XZONE GOLD Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEXY MONKEY Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MiracleZEN Platinum Recalled by Schindele Enterprises dba Midwest Wholesale...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XZEN PLATINUM Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 Recalled by Hospira...
The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminosyn 3.5% M Sulfite-Free Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ExtenZe 600 mg Recalled by Schindele Enterprises dba Midwest Wholesale Due...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magic For Men Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BOOST ULTRA Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Smith & Nephew RENASYS-Gauze with Soft Port Kit REF #'s: 66800933 Recalled...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-F XL with Soft Port REF #: Recalled by Smith & Nephew...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-F Foam Dressing Kit with Soft Port REF #'s: 66800794...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Recalled...
The Issue: Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products White Slides Recalled by Ortho-Clinical...
The Issue: An incorrect assay value (0.3785) was printed on the product carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Multicompartmental Knee (MCK) System is an implant system designed...
The Issue: The product may be mislabeled and could result in the incorrect implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-G Sterile Recalled by Smith & Nephew Inc. Due to...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.