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. 2,786 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,786 in last 12 months

Showing 1430114320 of 53,623 recalls

FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: Dole 12 oz American / Melange Americain SKU: 687 Recalled by Dole Fresh...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: Little Salad Bar 9 oz Italian Salad SKU: 3215 Recalled by Dole Fresh...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: Marketside 24 oz Classic Iceberg Salad SKU: 3193 Recalled by Dole Fresh...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: Marketside 12 oz Crisp Greens SKU: 3265 Recalled by Dole Fresh Vegetables...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: Dole 8oz Shredded Lettuce SKU: 2029 Recalled by Dole Fresh Vegetables Inc...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: Marketside 12oz Crisp Greens SKU: 3265 Recalled by Dole Fresh Vegetables Inc...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: Dole 11oz Greener Selection SKU: 34 Recalled by Dole Fresh Vegetables Inc...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 6, 2022· Dole Fresh Vegetables Inc

Recalled Item: HEB 8oz Shredded Lettuce SKU: 3308 Recalled by Dole Fresh Vegetables Inc Due...

The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 6, 2022· World Health Products LLC

Recalled Item: GAT SPORT JETFUEL DIURETIC Recalled by World Health Products LLC Due to...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 6, 2022· Philips North America

Recalled Item: Ingenia Ambition X (Product Number 781356) - HA FlexTrak II Recalled by...

The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2022· Philips North America

Recalled Item: Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Recalled by...

The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2022· Philips North America

Recalled Item: Ingenia Elition X (Product Number 781358) - HA FlexTrak II Recalled by...

The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2022· Becton Dickinson & Company

Recalled Item: BD Vacutainer Luer Lok Access Device - intended as a sterile Recalled by...

The Issue: May shed contaminant particles into the urine specimen that may be...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 6, 2022· Envisiontec US Llc

Recalled Item: FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth...

The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2022· Envisiontec US Llc

Recalled Item: FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth...

The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...

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

Class II — Potential Health HazardOngoing
DrugJanuary 5, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Semglee (insulin glargine) injection Recalled by Mylan Pharmaceuticals Inc...

The Issue: Labeling: Missing Label: label missing from some Semglee prefilled pens.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 5, 2022· Akorn, Inc.

Recalled Item: Sufentanil Citrate Injection Recalled by Akorn, Inc. Due to Subpotent Drug:...

The Issue: Subpotent Drug: Out of specification for assay at the 30-month stability...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 5, 2022· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Recalled...

The Issue: May have adhesive residue on the posterior surface of the femoral augment,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2022· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as Recalled by...

The Issue: May have adhesive residue on the posterior surface of the femoral augment,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2022· Becton Dickinson & Co.

Recalled Item: BD Veritor Plus Analyzer - intended to provide rapid test Recalled by Becton...

The Issue: May have the potential to overheat and/or cause fire, the issue can occur...

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

Class II — Potential Health HazardOngoing