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 22012220 of 29,154 recalls

Medical DeviceFebruary 3, 2025· Beckman Coulter, Inc.

Recalled Item: Access Erythropoietin (EPO) Recalled by Beckman Coulter, Inc. Due to...

The Issue: Affected lot (439363) exhibited a negative dose drop of -22% with native...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· American Contract Systems, Inc.

Recalled Item: Brand Name: Banner University Med Ctr. Product Name: Cardiac Cath Recalled...

The Issue: Sterility assurance with procedure trays

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· American Contract Systems, Inc.

Recalled Item: Brand Name: Banner Health Systems Product Name: Cysto Pack Model/Catalog...

The Issue: Sterility assurance with procedure trays

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· American Contract Systems, Inc.

Recalled Item: Brand Name: Banner Health Systems Product Name: Lap Pack - Recalled by...

The Issue: Sterility assurance with procedure trays

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: SIGNA MR355 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...

The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: Paradigm and MMT-715 Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: Paradigm insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: Paradigm insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing