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. 2,802 recalls have been distributed to Arizona in the last 12 months.
Showing 361–380 of 29,154 recalls
Recalled Item: Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene C. difficile Recalled by Meridian Bioscience Inc Due to The...
The Issue: The affected lots show a decline in performance over time, which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Leos Laser and Endoscopy System. Model Number: OME6000U. Recalled by...
The Issue: Manufacturing deviation in which the ferrites specified for the USB cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Recalled by...
The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abre Venous Self-Expanding Stent System Recalled by Medtronic Inc Due to...
The Issue: Stents may be impacted by a Nitinol anomaly which causes a reduced stent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allwell Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Recalled...
The Issue: Due to probe bags that may have a compromised or incomplete sterile pouch seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allwell Angioplasty Pack /B Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Numbers:...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography...
The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and...
The Issue: Complaints received that Vanta A71200 CP App does not function as intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T. Product Code (REF): (1) 781341 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter...
The Issue: Boston Scientific is initiating the removal of certain batches of Coyote"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis ES Enterprise Server Catalog Numbers 1115-00 Recalled by CareFusion...
The Issue: Due a software issue that may result in equipment not receiving timely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade to MR 7700. Product Code (REF): 782130. MR systems Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S. Product Code (REF): (1) 781357 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.