Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,858 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,858 in last 12 months

Showing 34013420 of 53,623 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· 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
Medical DeviceJanuary 30, 2025· Telcare, LLC

Recalled Item: Philips Connected Blood Glucose Meter Recalled by Telcare, LLC Due to...

The Issue: Telcare, LLC has received customer complaints related to battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2025· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Brand Name: Leica Biosystems Cryostats Product Name: CM1950 Model/Catalog...

The Issue: Firm became aware of software issues related to most recent firmware update...

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Atomoxetine Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA...

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

Class II — Potential Health HazardOngoing
Refund