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. 1,922 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,922 in last 12 months

Showing 2926129280 of 53,623 recalls

Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: VALITUDE X4 CRT-P Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
DrugDecember 7, 2017· BotanicalNow

Recalled Item: BodySlim Herbal Advanced technology & Strong formula capsules Recalled by...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena Acne Proofing whipped foam cleanser Recalled by Johnson & Johnson...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena deep clean purifying whipped foam cleanser Recalled by Johnson &...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· SCA Pharmaceuticals

Recalled Item: Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - product label was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 6, 2017· Reliance Medical Products Inc

Recalled Item: Suspension Arm (P/N: 525004 Recalled by Reliance Medical Products Inc Due to...

The Issue: Product has been found with a missing Washer, Retaining Ring, and/or Stop...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2017· Intel-GE Care Innovations LLC

Recalled Item: Health Harmony Mobile application software Product Usage: Care Innovations...

The Issue: It was discovered that in certain situations, including partial sessions and...

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

Class II — Potential Health HazardOngoing
DrugDecember 5, 2017· Sanofi-Aventis U.S. LLC

Recalled Item: Enoxaparin Sodium Recalled by Sanofi-Aventis U.S. LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. A single syringe labeled as 150...

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

Class III — Low RiskOngoing
Refund
FoodDecember 5, 2017· Aldi Inc

Recalled Item: Choceur Dark Chocolate Bars Recalled by Aldi Inc Due to Undeclared Treenut

The Issue: ALDI has voluntarily recalled Choceur Dark Chocolate Bars due to the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 5, 2017· Creative Contract Packaging Corporation, LLC

Recalled Item: HERB-OX Beef Flavor Granulated Bouillon Recalled by Creative Contract...

The Issue: Creative Contract Packaging LLC is voluntarily recalling two code dates of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Truth Renew Recalled by Accord Media, LLC Due to Distribution of medical...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Ultra Renew Plus Recalled by Accord Media, LLC Due to Distribution of...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Beckman Coulter Inc.

Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...

The Issue: A subset of Lot 7212154 A of the iChem VELOCITY Urine Chemistry strips has...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Smiths Medical ASD Inc.

Recalled Item: PORT-A-CATH II PS/Titan Recalled by Smiths Medical ASD Inc. Due to Certain...

The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Truth Renew Plus Recalled by Accord Media, LLC Due to Distribution of...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Cellavision AB

Recalled Item: CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the Recalled by...

The Issue: A software malfunction was found where WBC, RBC and PLT comments added after...

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

Class II — Potential Health HazardOngoing