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. 2,905 recalls have been distributed to Texas in the last 12 months.
Showing 3241–3260 of 55,713 recalls
Recalled Item: Baxter Floor mounting column TS 7500 U Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Mobile column TruSystem 7500 Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Livalo (pitavatstatin) tablets Recalled by Kowa Pharmaceuticals America Due...
The Issue: Presence of foreign tablets/capsules
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zapzyt Recalled by Denison Pharmaceuticals, LLC Due to Chemical...
The Issue: Chemical Contamination: Presence of benzene.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.) Market Pantry Soup & Oyster Crackers Recalled by Shearer's Foods, LLC...
The Issue: Potential foreign material (stainless steel wire)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) Recalled by...
The Issue: The firm received complaints of spoilage and illness with the use of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL...
The Issue: The firm received complaints of spoilage and illness with the use of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medical convenience kits containing Medtronic Aortic Root Cannula are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medical convenience kits containing Medtronic Aortic Root Cannula are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline medical procedure kits, containing Medtronic Aortic Root Cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medical convenience kits containing Medtronic Aortic Root Cannula are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitality Recalled by One Source Nutrition, Inc, Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Connecta BD Luer-Lok 360 Recalled by BD SWITZERLAND SARL Due to Due to...
The Issue: Due to specific lots of luer-lok devices were shipped to the U.S. market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...
The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...
The Issue: The RSV target may give a late Ct value and could potentially not pass QC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.