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. 2,798 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,798 in last 12 months

Showing 541560 of 52,339 recalls

DrugDecember 8, 2025· Signature Formulations, LLC

Recalled Item: ORL Kids Mouthwash Recalled by Signature Formulations, LLC Due to cGMP...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2025· Signature Formulations, LLC

Recalled Item: ORL Kids Natural Toothpaste Recalled by Signature Formulations, LLC Due to...

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 8, 2025· Beckman Coulter Ireland, Inc.

Recalled Item: The LDL-Cholesterol assay is comprised of two distinct phases. In Recalled...

The Issue: Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Systems R3.0. Includes the following label descriptions and...

The Issue: Nine (9) identified software issues which may result in the following: loss...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2025· IMRIS Imaging Inc

Recalled Item: Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog...

The Issue: Torque screw may crack or separate. If used, an affected screw could lead to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2025· Securitas Healthcare LLC

Recalled Item: Arial 900 MHz Call Station Recalled by Securitas Healthcare LLC Due to...

The Issue: Securitas Healthcare has become aware of a firmware issue in the Call...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2025· Securitas Healthcare LLC

Recalled Item: Arial 900 MHz Call Station Recalled by Securitas Healthcare LLC Due to...

The Issue: Securitas Healthcare has become aware of a firmware issue in the Call...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2025· LimFlow, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2025· Meridian Bioscience Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2025· Beaver-Visitec International, Inc.

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.

Class II — Potential Health HazardOngoing
FoodDecember 4, 2025· AZ Gems, Inc.

Recalled Item: Jumbo RAW SHRIMP Recalled by AZ Gems, Inc. Due to elevated levels of...

The Issue: elevated levels of chloramphenicol in frozen shrimp

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Intuitive Surgical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Mobius Imaging, LLC

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.

Class II — Potential Health HazardOngoing