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. 2,771 recalls have been distributed to Arizona in the last 12 months.
Showing 6021–6040 of 52,339 recalls
Recalled Item: Philips Interventional Hemodynamic Application R.1.2X Recalled by PHILIPS...
The Issue: Potential for pressure wave data synchronization from two devices may not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirolimus Tablets 1mg Tablets 100-count bottle Recalled by Dr. Reddy's...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meijer Magnesium Citrate Saline Laxative Oral Solution Dye Free Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Recalled...
The Issue: Microbial Contamination of Non-Sterile Products - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous...
The Issue: Internal product testing failed bubble leak testing (ASTM F2096), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardura XL (doxazosin) extended release tablets 8mg Recalled by Viatris Inc...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardura XL (doxazosin) extended release tablets 4mg Recalled by Viatris Inc...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection Recalled...
The Issue: Labeling: Wrong Barcode
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZOLL 731 Ventilator (EMV+ Recalled by ZOLL Medical Corporation Due to...
The Issue: Operator's Guide & Quick Guide (QRG) ZOLL 731 Ventilator for MRI Compatible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TabloCart with Prefiltration Drawer PN-0006813 Recalled by Outset Medical,...
The Issue: A cart with prefiltration drawer, an optional hemodialysis system accessory,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD (case) and DYNJ04049H Recalled by...
The Issue: There is the potential of the tip protector to fall off 4.5" sterile,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BSM-3000 Series Bedside Monitor The Life Scope BSM-3000 Recalled by Nihon...
The Issue: Due to software issue the device may give false "SpO2 Probe Failure" alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow UltraFlex Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437...
The Issue: Due to software issues, their is the potential for loss of image or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404...
The Issue: Due to software issues, their is the potential for loss of image or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.