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. 934 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
934 in last 12 months

Showing 53001–53020 of 53,623 recalls

FoodMay 4, 2012· FunFresh Foods Inc

Recalled Item: FunFresh Foods World Berry Organic Cacao Nibs 6 oz Recalled by FunFresh...

The Issue: FunFresh Foods World Berry Cacao Nibs 6 oz snack food contaminated with E. coli.

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

Class III — Low RiskOngoing
Refund
FoodMay 4, 2012· Snyder's - Lance Inc.

Recalled Item: Tom's Bacon Cheddar Fries Recalled by Snyder's - Lance Inc. Due to...

The Issue: Product contains undeclared certified colors (Yellow #6, Red #40, Yellow#6...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 5% Dextrose Injection USP Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 20% Dextrose Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 70% Dextrose Injection USP Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 1.5% Glycine Irrigation Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 3, 2012· Arrow International Inc

Recalled Item: Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R)...

The Issue: Lidstock of product does not contain chlorhexidine contraindication and...

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

Class I — Serious Health HazardOngoing
DrugMay 2, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Zeosa (norethindrone and ethinyl estradiol tablets USP Recalled by Teva...

The Issue: Impurities/Degradation: This recall is being carried out due to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2012· Ben Venue Laboratories Inc

Recalled Item: Octreotide Acetate Injection Recalled by Ben Venue Laboratories Inc Due to...

The Issue: Short Fill: These products are being recalled because there is potential...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2012· Ben Venue Laboratories Inc

Recalled Item: Midazolam HCl Injection Recalled by Ben Venue Laboratories Inc Due to Short...

The Issue: Short Fill: These products are being recalled because there is potential...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical NUVO LITE MODEL 525 OCSI Recalled by Nidek Medical Products...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical MARK5 NUVO 8 /OCSI Recalled by Nidek Medical Products Inc Due...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical M5C5/ MARK5 NUVO/OCSI Recalled by Nidek Medical Products Inc...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical NUVO LITE MODEL 925 OCSI Recalled by Nidek Medical Products...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical M5C5/ MARK5 NUVO/STD Recalled by Nidek Medical Products Inc...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing