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. 2,550 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,550 in last 12 months

Showing 4570145720 of 53,623 recalls

DrugApril 25, 2014· Prestige Brands Holdings

Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...

The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...

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

Class III — Low RiskOngoing
Refund
FoodApril 25, 2014· Kroger Co

Recalled Item: Private Selection Chocolate Hazelnut Mascarpone Ice Cream Recalled by Kroger...

The Issue: The firm discovered that the label for two of their products did not declare...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 25, 2014· Kroger Co

Recalled Item: Private Selection Caramel Hazelnut Fudge Truffle Ice Cream Recalled by...

The Issue: The firm discovered that the label for two of their products did not declare...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 25, 2014· Hitachi Medical Systems America Inc

Recalled Item: Oasis Coil Extension Cable used with Hitachi Oasis MRI System Recalled by...

The Issue: The firm received a complaint stating the Coil Extension Cable accessory...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...

The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· CryoLife, Inc.

Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...

The Issue: Serum albumin component monomer failed to meet internally established end of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: MAMMOMAT Inspiration. Intended for mammography exams Recalled by Siemens...

The Issue: There is a potential and possible hazard to the user when using the MAMMOMAT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...

The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...

The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...

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

Class II — Potential Health HazardOngoing
DrugApril 24, 2014· Baxter Healthcare Corp.

Recalled Item: Famotidine Injection 20 mg Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Baxter Healthcare Corporation has received a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2014· Stonyfield Farm

Recalled Item: Stonyfield YoBaby Vanilla Organic Whole Milk Yogurt multipack 6 pack...

The Issue: Product has elevated levels of coliforms

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2014· Stonyfield Farm

Recalled Item: Stonyfield YoToddler Raspberry/Pear Cereal Organic Whole Milk Yogurt with...

The Issue: Product has elevated levels of coliforms

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2014· Stonyfield Farm

Recalled Item: Stonyfield YoBaby Pear/Peach Organic Whole Milk Yogurt multipack- 6 pack...

The Issue: Product has elevated levels of coliforms

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 24, 2014· Baxter Healthcare Corp.

Recalled Item: Baxter Amia Automated PD systems are used in the treatment Recalled by...

The Issue: System error 01779 is produced when the battery cannot be charged due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: UPGRD PRGM 9734638 ADD AxiEM NAVIGATION Recalled by Medtronic Navigation,...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: DRAPE 9732722 TUBE STERILE O-ARM 20PK Recalled by Medtronic Navigation, Inc....

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: TUMOR RES. PACK 9733553 AxiEM S.M. Recalled by Medtronic Navigation, Inc....

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing