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. 2,759 recalls have been distributed to Arizona in the last 12 months.
Showing 8001–8020 of 29,154 recalls
Recalled Item: Various neurology packs Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Pacemaker Packs Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various ENT Packs Recalled by American Contract Systems, Inc. Due to Product...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Angiography/Cath Lab packs/trays Recalled by American Contract...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Cysto Packs Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various hysterectomy Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Laparoscopy Packs Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various PICC Line Recalled by American Contract Systems, Inc. Due to Product...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicBrainEX Recalled by NordicNeuroLab AS Due to When exporting merged...
The Issue: When exporting merged results from the BOLD, DSC, and DCE modules of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARS CoV 2 rapid antigen test kits packaged under the Recalled by North...
The Issue: Various brands of SARS CoV 2 Antigen Rapid Test kits were offered for sale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis with software version VD12A. A diagnostic and administrative tool...
The Issue: Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe Combo with software version VD12A. A diagnostic and Recalled by...
The Issue: Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS Software Version 7.0 SP0.0.4.7 Recalled by GE Healthcare,...
The Issue: The Event Notification Manager (ENM) functionality for certain products does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sight OLO Recalled by SIGHT DIAGNOSTICS LTD Due to The default ranges for...
The Issue: The default ranges for MCH, MCHC, and RDW for age group "Child 2-11y" are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative...
The Issue: The Instructions for Use (IFU, Part Number 750095) provided with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wright EVOLVE TRIAD Plate Cutter Recalled by Wright Medical Technology, Inc....
The Issue: The plate cutter is unable to meet sterilization requirements when it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeGlobal Fast Freeze Thawing Kit Recalled by CooperSurgical, Inc. Due to...
The Issue: There was translation error in the Spanish version of the IFU where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haiou Needle Retractable Safety Syringe with Needle-1ML 23G x 1 Recalled by...
The Issue: Complaints received in which needle and needle holder have detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.