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 25412560 of 52,339 recalls

FoodMay 10, 2025· Fresh & Ready Foods LLC

Recalled Item: Fresh & Ready Foods Turkey & Cheese Mega Sandwich Recalled by Fresh & Ready...

The Issue: Listeria Monocytogenes detected on food contact surfaces in Ready To Eat...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 10, 2025· Fresh & Ready Foods LLC

Recalled Item: Fresh & Ready Foods Caprese Baguette Recalled by Fresh & Ready Foods LLC Due...

The Issue: Listeria Monocytogenes detected on food contact surfaces in Ready To Eat...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 10, 2025· Fresh & Ready Foods LLC

Recalled Item: Fresh & Ready Foods Egg Salad on Wheat Sandwich Recalled by Fresh & Ready...

The Issue: Listeria Monocytogenes detected on food contact surfaces in Ready To Eat...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 10, 2025· Fresh & Ready Foods LLC

Recalled Item: Fresh & Ready Foods Ham & Cheese Sub Sandwich Recalled by Fresh & Ready...

The Issue: Listeria Monocytogenes detected on food contact surfaces in Ready To Eat...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 9, 2025· AvKARE

Recalled Item: Chlorthalidone Tablets Recalled by AvKARE Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 9, 2025· Alembic Pharmaceuticals Limited

Recalled Item: Celecoxib Capsules Recalled by Alembic Pharmaceuticals Limited Due to...

The Issue: Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 9, 2025· KVK Tech, Inc.

Recalled Item: Indomethacin Extended-Release Capsules USP Recalled by KVK Tech, Inc. Due to...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 9, 2025· KVK Tech, Inc.

Recalled Item: Phentermine Hydrochloride Capsules Recalled by KVK Tech, Inc. 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
Medical DeviceMay 9, 2025· Philips Respironics, Inc.

Recalled Item: BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for...

The Issue: This device does not indicate for use in patients with respiratory failure.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Recalled by Ortho-Clinical Diagnostics, Inc. Due to a...

The Issue: a software anomaly allows test results to be reported using Micro Tip and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2025· Philips Respironics, Inc.

Recalled Item: BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory...

The Issue: This device does not indicate for use in patients with respiratory failure.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2025· Philips Respironics, Inc.

Recalled Item: BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support...

The Issue: This device does not indicate for use in patients with respiratory failure.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog...

The Issue: a software anomaly allows test results to be reported using Micro Tip and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...

The Issue: A software anomaly allows test results to be reported using Micro Tip and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2025· Barco N.V.

Recalled Item: Model: Description/: MNA-420 ENC -H/K9303320 Recalled by Barco N.V. Due to...

The Issue: Cathode ray tube display system encoders and decoders have same MAC address;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2025· Baxter Healthcare Corporation

Recalled Item: 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope...

The Issue: The replacement rechargeable batteries inserted into the Welch Allyn...

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

Class II — Potential Health HazardOngoing
FoodMay 8, 2025· Now Foods

Recalled Item: NOW Nutritional Yeast Powder Recalled by Now Foods Due to regular yeast was...

The Issue: regular yeast was inadvertently packaged as nutritional yeast

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 8, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis Product Name / UDI-DI code / Catalog No. Recalled by CareFusion...

The Issue: Antivirus software was not consistently installed on impacted devices during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2025· CareFusion 303, Inc.

Recalled Item: Product Name [REF]: Supply Server Recalled by CareFusion 303, Inc. Due to...

The Issue: During automated dispensing cabinet upgrade/installation/reimaging,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2025· Ohio Medical Corporation

Recalled Item: GCE HEALTHCARE Zen-O lite Recalled by Ohio Medical Corporation Due to...

The Issue: Erroneous calibration values, potentially resulting in: as the device ages,...

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

Class II — Potential Health HazardOngoing