Product Recalls in Arizona
Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,420 recalls have been distributed to Arizona in the last 12 months.
Showing 39421–39440 of 52,339 recalls
Recalled Item: Metro Market Lemon Pepper Rub Recalled by Regency Group, Inc., The Due to...
The Issue: Metro Market Lemon Pepper Rub is recalled due to contamination with gluten...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pizza Seasoning Recalled by Regency Group, Inc., The Due to Pizza Seasoning...
The Issue: Pizza Seasoning is recalled due to contamination with gluten (wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Turtle Island Roast Beef Spice Blend Recalled by Regency Group, Inc., The...
The Issue: Turtle Island Roast Beef Spice Blend is recalled due to contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taco Seasoning No Salt Recalled by Regency Group, Inc., The Due to Taco...
The Issue: Taco Seasoning No Salt is recalled due to contamination with gluten (wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: French Fry Seasoning Recalled by Regency Group, Inc., The Due to French Fry...
The Issue: French Fry Seasoning is recalled due to contamination with gluten (wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: I-Portal¿ NOTC and VNG Recalled by Neuro Kinetics, Inc. Due to complaints of...
The Issue: complaints of system malfunction and unintended, sudden movement at start...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended...
The Issue: Sterility of device maybe compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRI Femoral Impactor Block for knee prosthesis surgery. Orthopedic Manual...
The Issue: Potential for uncured adhesive between the metal threaded insert and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit Recalled by Mission...
The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint...
The Issue: Maxivision MaxiFlex (Registered) Multinutrient Formula, 120 Vegetable...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fajita Seasoning Recalled by Regency Group, Inc., The Due to Fajita...
The Issue: Fajita Seasoning is recalled due to contamination with gluten (wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...
The Issue: Complaints with the HVAD Abnormal Power Source Switching.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink Data Management System Recalled by Siemens Healthcare Diagnostics,...
The Issue: System Limitations and Software Issues related to the following features:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: Complaints with the HVAD Internal Controller Alarm Battery failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...
The Issue: Complaints with the HVAD Discolored and Cracked Driveline Outer Sheath.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #: 1101 Recalled by...
The Issue: Complaints with the HVAD Retraction of Pins within the driveline connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: HeartWare has received complaints relating to damage or bent connection pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail...
The Issue: The entire scope of 4.5mm Cortical Screws listed as compatible with the M/DN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lerner Laboratories Mucolexx Recalled by Richard-Allan Scientific Company...
The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.