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. 2,602 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,602 in last 12 months

Showing 3966139680 of 53,623 recalls

DrugAugust 6, 2015· Blue Square Market, Inc.

Recalled Item: LiDa DAIDAIHUA (also packaged as LiDa DAIDAIHUAJIAONANG) Recalled by Blue...

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
FoodAugust 6, 2015· Caribou Coffee Company Inc.

Recalled Item: Caribou Chocolate Chip Toffee Pecan Biscotti Recalled by Caribou Coffee...

The Issue: Biscotti Almond and Biscotti Chocolate Chip Toffee Pecan are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 6, 2015· Caribou Coffee Company Inc.

Recalled Item: Caribou Almond Biscotti Recalled by Caribou Coffee Company Inc. Due to...

The Issue: Biscotti Almond and Biscotti Chocolate Chip Toffee Pecan are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 5, 2015· Brainlab AG

Recalled Item: ExacTrac 6.0.x Patient Positioning System Recalled by Brainlab AG Due to...

The Issue: ExacTrac 6.0 Patient Positioning System: Display of potentially incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2015· Leica Microsystems, Inc.

Recalled Item: The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology...

The Issue: The Leica ASP200S/ASP300S Tissue Processor have an incorrect internal wiring...

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

Class III — Low RiskOngoing
Medical DeviceAugust 5, 2015· Natus Medical Incorporated

Recalled Item: Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy Recalled by...

The Issue: The neoBLUE Instruction For Use (IFU) and Service Manuals for the neoBLUE 3...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to A software fix...

The Issue: A software fix has been released to prevent automatic movement resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2015· Biomet Spine, LLC

Recalled Item: Biomet Parsippany Recalled by Biomet Spine, LLC Due to Mislabeling

The Issue: Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.

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

Class II — Potential Health HazardOngoing
DrugAugust 5, 2015· Taro Pharmaceuticals, Inc.

Recalled Item: Topicort (desoximetasone) Topical Spray Recalled by Taro Pharmaceuticals,...

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

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 4, 2015· Bayer Healthcare

Recalled Item: Angiographic Injector. Medrad Mark 7 Arterion Injection System Recalled by...

The Issue: Software Version SW 005.006_SH, resulted in the removal of purge enforcement...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2015· MicroPort Orthopedics, Inc.

Recalled Item: PROFEMUR PLUS CoCr MODULAR NECK Recalled by MicroPort Orthopedics, Inc. Due...

The Issue: Unexpected rate of postoperative fractures resulting in the need for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2015· Salter Labs

Recalled Item: NebuTech Nebulizer Recalled by Salter Labs Due to The Inspiratory valve cap...

The Issue: The Inspiratory valve cap on the nebulizer reservoir tower may be loose and...

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

Class II — Potential Health HazardOngoing
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Golden Seal Extract packaged in 1 FL OZ (29mL) droppers. HoneyCombs...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Expello-C packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula L packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula C&F packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula IM packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 3, 2015· Liquid Coffee Inc

Recalled Item: Concentrated coffee packed in 1/2 gallon or 1 gallon hermetically Recalled...

The Issue: The pH level in coffee product was elevated above 4.6.

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

Class II — Potential Health HazardOngoing
Refund