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 3050130520 of 53,623 recalls

Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Straight Suction 9733449 EM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Curved Suction 70 9733450 EM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Instrument Kit 9733908 Fusion ENT Recalled by Medtronic...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Set Supplemental INS AxiEM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Curved Suction 90 9733451 EM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Suction 9734308 Small AxiEM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Instrument Set EM ENT Recalled by Medtronic Navigation, Inc. Due...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: Obagi-C Rx System C-Therapy Night Cream Recalled by Valeant Pharmaceuticals...

The Issue: Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy...

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2017· GSK Consumer Healthcare

Recalled Item: parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and...

The Issue: Presence of Foreign Substance: possibility of the presence of metal in the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 28, 2017· Kettle Foods, Inc.

Recalled Item: Kettle Brand Krinkle Cut Potato Chips Spicy Queso Recalled by Kettle Foods,...

The Issue: Carbohydrates on nutritional facts panel are stated as 3g/serving when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 27, 2017· Peanut Butter holdings, LLC

Recalled Item: PB Crave Recalled by Peanut Butter holdings, LLC Due to Mislabeling

The Issue: Product mislabeled. "'Contains " allergen statement under the ingredient...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety Deluxe Bone Marrow Biopsy/Aspiration Tray Recalled by Robert Busse &...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Laceration Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle Recalled...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System Recalled by...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

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

Class II — Potential Health HazardOngoing