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. 1,122 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,122 in last 12 months

Showing 6861–6880 of 52,339 recalls

FoodFebruary 5, 2024· Sargento Foods, Inc.

Recalled Item: Sargento Bevel Shredded Queso Quesadilla Cheese. Pack Size 450/1 oz....

The Issue: Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2024· Sargento Foods, Inc.

Recalled Item: Parmesan cheese packaged in the following configurations: 1. Sargento Fresh...

The Issue: Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2024· Sargento Foods, Inc.

Recalled Item: Monterey Jack cheese packaged in the following configurations: 1. Sargento...

The Issue: Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 2, 2024· Bausch Health Companies, Inc.

Recalled Item: Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1 Recalled by...

The Issue: Subpotent Drug: Out of specification for assay

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with Recalled by...

The Issue: Pack and pouch label is missing the manufacturing and expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: Wash station: M1000 Wash Station Assembly & DITI Slide Recalled by Abbott...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis: MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing cabinets, running affected software, and Windows 10...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis LSI ATM (11q22.3) SpectrmOrange...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
DrugFebruary 1, 2024· Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Recalled Item: TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid Recalled by...

The Issue: Chemical Contamination; presence of benzene.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2024· Integrity Products

Recalled Item: To the Moon Capsules Recalled by Integrity Products Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2024· Integrity Products

Recalled Item: RAM IT Recalled by Integrity Products Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2024· Amerisource Health Services LLC

Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Amerisource Health Services...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 1, 2024· NATCO Pharma Limited

Recalled Item: Lansoprazole Delayed-Release Capsules USP Recalled by NATCO Pharma Limited...

The Issue: CGMP Deviations: Inadequate induction sealing on bottles, capsules were...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 1, 2024· House of Coffee Beans, Inc

Recalled Item: Coffee 5 pound bags Recalled by House of Coffee Beans, Inc Due to potential...

The Issue: potential allergen contact with almonds, pecans and coconut.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD used to calibrate the...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2024· Technicality Inc.

Recalled Item: Trumpet Recalled by Technicality Inc. Due to The Ring on the Trump Needle...

The Issue: The Ring on the Trump Needle Guide can detach when excessive pressure is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Applied Medical Resources Corp

Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...

The Issue: Their is the potential that Universal Clip applier may not load clip after...

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

Class II — Potential Health HazardOngoing