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 2944129460 of 53,623 recalls

DrugNovember 11, 2017· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Superpotent

The Issue: Superpotent

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2017· Baxter Healthcare Corporation

Recalled Item: Nexterone (amiodarone HCl) Premixed Injection Recalled by Baxter Healthcare...

The Issue: Presence of Particulate Matter:Particulate identified as polyethylene, the...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 10, 2017· New Century Snacks LLC

Recalled Item: Happy Belly Deluxe Mixed Nuts - roasted and salted with sea salt. Cashews...

The Issue: Firm was notified by customer that the back panel (ingredients and nutrition...

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

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2017· New Century Snacks LLC

Recalled Item: Happy Belly Cranberry & Nuts Trail Mix - dried cranberries Recalled by New...

The Issue: Firm was notified by customer that the back panel (ingredients and nutrition...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 10, 2017· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution - Premixed Dialysate for Hemodialysis with...

The Issue: Using different fluid formulations of NxStage PureFlow B Solution at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Beckman Coulter Inc.

Recalled Item: iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100...

The Issue: iQ200 Series Urine Microscopy Analyzer may intermittently fail to read urine...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· C.R. Bard, Inc.

Recalled Item: CritiCore Automated Urine Output and Temperature Monitor Recalled by C.R....

The Issue: Issues identified with the monitor including urine output measurement...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2017· Vascular Insights, LLC

Recalled Item: ClariVein IC infusion catheter Recalled by Vascular Insights, LLC Due to...

The Issue: Certain catheters could have a compromised catheter shaft due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista System LOCI 8 CALIBRATOR The LOCI 8 Calibrator Recalled by...

The Issue: An increase in the number of failed calibration events or negative bias with...

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

Class II — Potential Health HazardOngoing
DrugNovember 9, 2017· Mayne Pharma Inc

Recalled Item: Liothyronine Sodium Tablets Recalled by Mayne Pharma Inc Due to Failed...

The Issue: Failed Dissolution Specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2017· Teva Pharmaceuticals USA

Recalled Item: Clozapine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Tablet/Capsule Specifications; potential presence of broken tablets.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2017· Kareway Products Inc

Recalled Item: GERICARE Eyewash Recalled by Kareway Products Inc Due to Non-sterility:...

The Issue: Non-sterility: confirmed microbial contamination with Achromobacter xylosoxidans

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 9, 2017· Figi's, Inc

Recalled Item: Dark Chocolate covered Gingersnaps. Packaged as follows: 1. in clear...

The Issue: Figi's is recalling Gift #0368 Christmas Gingersnap Variety and Bulk Dark...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 8, 2017· Bard Medical Division

Recalled Item: Medivance(R) ARCTIC SUN(R) ARCTICGEL(TM) Pads: Description Recalled by Bard...

The Issue: Specific lots of ArcticGel Pads have potential issues which may result in...

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

Class II — Potential Health HazardOngoing