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. 1,029 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,029 in last 12 months

Showing 36501–36520 of 53,623 recalls

FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Diced Carrots Recalled by CRF Frozen Foods, LLC Due to Potential Listeria...

The Issue: Carrots are recalled because they have the potential to be contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· SunOpta Food and Grain, Inc.

Recalled Item: 1. Roasted Not Salted Sunflower Kernel Recalled by SunOpta Food and Grain,...

The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· SunOpta Food and Grain, Inc.

Recalled Item: 1. Roasted & Salted Sunflower Kernel Recalled by SunOpta Food and Grain,...

The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· SunOpta Food and Grain, Inc.

Recalled Item: 2nd EXPANSION 5/31/2016 Navitas Naturals Recalled by SunOpta Food and Grain,...

The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· SunOpta Food and Grain, Inc.

Recalled Item: 2nd EXPANSION 5/31/2016 Blazin Hot sunflower kernel 1.2 oz. plastic Recalled...

The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· SunOpta Food and Grain, Inc.

Recalled Item: 2nd EXPANSION 5/31/2016 Product shipped OUS only. Light Salt Sunflower...

The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· SunOpta Food and Grain, Inc.

Recalled Item: 2nd EXPANSION 5/31/2016 Roasted No Salt Sweet Onion & White Recalled by...

The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 2, 2016· Leica Biosystems Richmond Inc.

Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...

The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...

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

Class III — Low RiskOngoing
Medical DeviceMay 2, 2016· AGFA Healthcare Corp.

Recalled Item: DX-D600 - DXD Imaging Package Recalled by AGFA Healthcare Corp. Due to One...

The Issue: One of the dent markers from the DX-D600 dropped down from the overhead rail.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...

The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...

The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...

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

Class II — Potential Health HazardOngoing
DrugMay 2, 2016· Sandoz, Inc

Recalled Item: Dicloxacillin Sodium Capsules USP Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...

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

Class III — Low RiskOngoing
Refund
DrugMay 2, 2016· Sandoz, Inc

Recalled Item: Dicloxacillin Sodium Capsules Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...

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

Class III — Low RiskOngoing
Refund
DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: BLACK GOLD X ADVANCED capsules Recalled by Making It a Lifestyle Due to...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing