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. 2,582 recalls have been distributed to Arizona in the last 12 months.
Showing 24361–24380 of 52,339 recalls
Recalled Item: 1 lb salted combo modjeskas Recalled by Bauer's Candies, Inc. Due to Risk of...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diatomaceous Earth packaged in the following ways: 1) Perma-Guard Recalled...
The Issue: Product contains elevated levels of lead, arsenic, and chromium: potentially...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROOT 23 CUCUMBER HABANERO SIMPLE SYRUP 375 ml Recalled by Root 23 LLC Due to...
The Issue: Non-compliance with process authority schedule; temperature at start of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Triton Sponge System (Software) Recalled by Stryker Instruments Div. of...
The Issue: Gauss Surgical is updating the Instructions for Use (IFU) for our Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiMobile UHMWPE Liner: ID-28mm/OD-54mm Recalled by Waldemar Link GmbH & Co....
The Issue: The internal labeling included with these implants may include incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiMobile UHMWPE Liner: ID-28mm/OD-50mm Recalled by Waldemar Link GmbH & Co....
The Issue: The internal labeling included with these implants may include incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 Recalled by...
The Issue: After an upgrade of the software of the Overhead Tube Crane, there were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Total Knee Replacement System Recalled by Conformis, Inc. Due to...
The Issue: The kits were prepared with incorrect patient ID labels and may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Controller Recalled by PENTAX of America Inc Due to The...
The Issue: The Controller does not detect overpressure in the balloon during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NYSTATIN Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Aurobindo Pharma USA...
The Issue: Discoloration: This product is being recalled due to a confirmed pharmacist...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has identified...
The Issue: GE Healthcare has identified that a small number of Nuclear Medicine systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has identified...
The Issue: GE Healthcare has identified that a small number of Nuclear Medicine systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion lnterventional Fluoroscopic X-ray System Recalled by Philips Medical...
The Issue: Philips has discovered through customer complaints and internal testing an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Visitec Soft Tip Cannula Recalled by Beaver Visitec Due to Certain lots...
The Issue: Certain lots are missing a protective sheath component over the silicone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Biograph Horizon PET/CT System Recalled by Siemens Medical Solutions...
The Issue: Improper design or specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK ACTH (ACTH: Adrenocorticotropic Hormone) is designed for IN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK Folate (FOL) is designed for IN VITRO DIAGNOSTIC USE Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Homocysteine (HCY) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Testosterone (TES) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.