Product Recalls in Vermont

Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,541 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,541 in last 12 months

Showing 30413060 of 47,027 recalls

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

Recalled Item: Optima MR360 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
DrugJanuary 30, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Potassium Chloride Extended-Release Tablets Recalled by The Harvard Drug...

The Issue: Failed Dissolution Specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 30, 2025· Micro Therapeutics, Inc.

Recalled Item: Medtronic Pipeline Vantage Embolization Device with Shield Technology...

The Issue: Use of embolization device with diameters greater-than-or-equal-to 4mm may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 30, 2025· Micro Therapeutics, Inc.

Recalled Item: Medtronic Pipeline Vantage Embolization Device with Shield Technology...

The Issue: Use of embolization device with diameters greater-than-or-equal-to 4mm may...

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

Class I — Serious Health HazardOngoing