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 15811600 of 29,154 recalls

Medical DeviceMay 22, 2025· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that...

The Issue: Investigation determined that one lot of the T2 Greater Trochanter Nail...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· LTS Therapy Systems, LLC

Recalled Item: IontoPatch STAT Recalled by LTS Therapy Systems, LLC Due to The nonwoven...

The Issue: The nonwoven pads in the device do not absorb the saline solution or any...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· LTS Therapy Systems, LLC

Recalled Item: IontoPatch 80 Recalled by LTS Therapy Systems, LLC Due to The nonwoven pads...

The Issue: The nonwoven pads in the device do not absorb the saline solution or any...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Cardiology Hemodynamics Software Recalled by CHANGE...

The Issue: Due to complaints, software update may cause software to unexpectedly shutdown.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Cardiology Hemo Software Recalled by CHANGE HEALTHCARE...

The Issue: Due to complaints, software update may cause software to unexpectedly shutdown.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· Jewel Precision Sheet Metal & Machining Co, Inc.

Recalled Item: Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog...

The Issue: The Instructions for Use do not match the 510(k) FDA cleared indications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....

The Issue: Devices contain potentially out-of-specification levels of endotoxins and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2025· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that...

The Issue: Investigation determined that one lot of the T2 Greater Trochanter Nail...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Product: Atellica CH Diluent - CONS 2 x 1.5L Recalled by Siemens Healthcare...

The Issue: Contamination of the diluent by sodium hypochlorite (NaOCl) which may impact...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....

The Issue: Devices contain potentially out-of-specification levels of endotoxins and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Insyte Autoguard Winged Shielded IV Catheter Recalled by Becton Dickinson...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Jolife AB

Recalled Item: LUCAS 2 Recalled by Jolife AB Due to Due to demonstration units of chest...

The Issue: Due to demonstration units of chest compression system being provided to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Covidien

Recalled Item: Newport HT70 Ventilator Recalled by Covidien Due to Ventilator Printed...

The Issue: Ventilator Printed Circuit Board Assembly may have two separate capacitors...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing