Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,768 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,768 in last 12 months

Showing 22012220 of 29,228 recalls

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: 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· 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· 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: 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· 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: Brivo 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· GE Healthcare (China) Co., Ltd.

Recalled Item: SIGNA MR380 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: 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: 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