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. 2,764 recalls have been distributed to Arizona in the last 12 months.
Showing 6821–6840 of 29,154 recalls
Recalled Item: Neodent GM X 6mm Engaging Titanium Base Recalled by Preat Corp Due to...
The Issue: Engaging titanium base contains a dimensional condition that allows vertical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD with RVD Enhancer: a) 1 mL Recalled by Entopsis , Inc....
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis BCSNano (1mL) Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Support: a) 1 mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD-RT Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Activator: a) 1.5mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent Buccal Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPerfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2D Perfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to There...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a...
The Issue: Battery leakage can cause corrosion to the metal enclosure near the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agilent Resolution ctDx FIRST Sample Collection Kit Recalled by AGILENT...
The Issue: Distributed sample collection kit with an unapproved instruction for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raystation treatment planning system for radiation therapy Recalled by...
The Issue: It is possible to set a non-zero collimator angle in the Virtual Simulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...
The Issue: An incorrect negative claim was identified on the claims page; the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flex-Neck Catheter External Repair Kit LOT CE-1400/A Recalled by Merit...
The Issue: Product that was built for design verification testing was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.