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. 2,562 recalls have been distributed to Arizona in the last 12 months.
Showing 32521–32540 of 52,339 recalls
Recalled Item: FH Parmesan. Product Code: T206486-50. 50 lb bags Recalled by All American...
The Issue: Products have been recalled due to potential for Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xtra Sharp Cheese Sauce. Product Code: T4015. 37.5 lb bags Recalled by All...
The Issue: Products have been recalled due to potential for Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chipotle Ranch ASI. Product Code: T3883. 33 lb bags Recalled by All American...
The Issue: Products have been recalled due to potential for Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: French Onion Seasoning ASI. Product Code: T3933. 33 lb bags Recalled by All...
The Issue: Products have been recalled due to potential for Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilbur Recalled by Cargill Cocoa & Chocolate, Inc. Due to Undeclared Milk
The Issue: Cargill Cocoa & Chocolate is recalling 50 lb. cartons of Wilbur B558...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DIAMONDBACK 360 Peripheral 1.50 Classic Recalled by Cardiovascular Systems...
The Issue: CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta International SA Recalled by Medacta Usa Inc Due to Damaged...
The Issue: Damaged packaging, lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Fixed Hinge Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INOVA (benzoyl peroxide) 4% Recalled by Cipher Pharmaceuticals US LLC Due to...
The Issue: Subpotent Drug: Product label claim is 4% Benzoyl Peroxide, Initial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT Recalled by...
The Issue: A breach in the sterile packaging may have occurred resulting in potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT...
The Issue: A breach in the sterile packaging may have occurred resulting in potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery Systems Recalled by Accuray Incorporated Due...
The Issue: Accuray has become aware of a potential safety issue involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentasa (mesalamine) Controlled-Release Capsules Recalled by Shire PLC Due...
The Issue: Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.