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 661680 of 29,154 recalls

Medical DeviceOctober 29, 2025· Philips North America Llc

Recalled Item: CT 5300 Recalled by Philips North America Llc Due to If the screws of tube...

The Issue: If the screws of tube heat exchanger on the rotating scanner are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2025· Illumina, Inc.

Recalled Item: Reagent Kits/ containing flow cells Recalled by Illumina, Inc. Due to An...

The Issue: An instrument intended for sequencing DNA libraries with in vitro diagnostic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn INF BAG Recalled by Baxter Healthcare Corporation Due to...

The Issue: Replacement bladder kit for the Welch Allyn two-piece reusable blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2025· Nipro Medical Corporation

Recalled Item: Hemodialysis System Recalled by Nipro Medical Corporation Due to Screw may...

The Issue: Screw may loosen or fallout of Hemodialysis system

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2025· Medline Industries, LP

Recalled Item: MEDLINE PERFUSION SYRINGE Recalled by Medline Industries, LP Due to Medline...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAMMOMAT Revelation Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: There were instances where the operator table was sold together with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM50...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Fetal & Maternal Monitor Model/Catalog...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: X8...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM8...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: elite...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iX10...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Telemetry Transmitter Model/Catalog Number:...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing