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. 2,643 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,643 in last 12 months

Showing 3144131460 of 53,623 recalls

FoodMay 11, 2017· Tyson Foods, inc.

Recalled Item: Sara Lee CP Quiche 10 Spinach Recalled by Tyson Foods, inc. Due to Potential...

The Issue: The firm is voluntarily recalling multiple lots of frozen Chef Pierre 10...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450 1.5T Product Usage: 1 .5T Brivo MR355 and Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system Recalled by...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDxt Recalled by GE Medical Systems, LLC Due to Possible...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDx Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: SIGNA Creator Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Discovery MR750 3.0T Product Usage: Intended use: The Discovery MR750...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Signa PET/MR (K163619 Recalled by GE Medical Systems, LLC Due to Possible...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Brivo MR355 Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Philips Electronics North America Corporation

Recalled Item: Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics...

The Issue: During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Teleflex Medical

Recalled Item: Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets...

The Issue: Product size listed on the labeling is incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Argon Medical Devices, Inc

Recalled Item: Clear Flashback Needle 7cm x 18G AMC/4 Recalled by Argon Medical Devices,...

The Issue: Argon Medical has received a complaint from one of their distributors of a...

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

Class II — Potential Health HazardOngoing
DrugMay 10, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· Medtronic Navigation, Inc.

Recalled Item: Install CD Recalled by Medtronic Navigation, Inc. Due to Software issue...

The Issue: Software issue related to the StealthStation S7 system and the Synergy Spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreather Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Masks Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing