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. 2,129 recalls have been distributed to Arizona in the last 12 months.
Showing 1261–1280 of 52,339 recalls
Recalled Item: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC FOCUS Shears + Adaptive Tissue Technology Recalled by Stryker...
The Issue: Due to manufacturing issue, reprocessed shears, may become stuck in the "on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...
The Issue: Failed impurity/degradation specifications:Out of Specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...
The Issue: Failed impurity/degradation specifications:Out of Specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Veritor Connect Software Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX System Recalled by Becton Dickinson & Co. Due to Product service...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix M50 Instrument Recalled by Becton Dickinson & Co. Due to Product...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic...
The Issue: Potential packaging issue that could compromise the sterile barrier. Defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sting Relief Swabs Recalled by ACME UNITED CORPORATION Due to Product Mix-up
The Issue: Product Mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD EpiCenter Microbiology Data Management System Recalled by Becton...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiWize Health OptiWize Collagen Plus 320 count bottle Recalled by Optiwize...
The Issue: The firm initiated a voluntary recall after NSF testing showed that labeled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Assay: IMMULITE 2000 Intact PTH Recalled by Siemens Healthcare Diagnostics,...
The Issue: The potential for falsely depressed Intact PTH patient results at the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxFLEX Flow Cytometer Catalog Number C78500 UDI-DI code: 15099590754013 The...
The Issue: Due to a software error code that crashes during acquisition on patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bevacizumab 1.75 mg/0.07 mL - 0.25 mL syringe Recalled by RC Outsourcing,...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 (net wt. 1 lbs/pkg Recalled...
The Issue: Shrimp may be contaminated with Cesium-137 (Cs-137).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kroger Raw Colossal EZ Peel Shrimp Recalled by Admiralty Island Fisheries...
The Issue: Shrimp may be contaminated with Cesium-137 (Cs-137).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AquaStar Raw Peeled Tail-on Shrimp Skewers Recalled by Admiralty Island...
The Issue: Shrimp may be contaminated with Cesium-137 (Cs-137).
Recommended Action: Do not consume. Return to store for a refund or discard.