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. 2,730 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,730 in last 12 months

Showing 1860118620 of 53,623 recalls

DrugSeptember 17, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 15 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: FDA analysis found these products to be less than the...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 17, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 120 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent...

The Issue: Subpotent Drug: FDA analysis found these products to be less than the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· Genicon, Inc.

Recalled Item: A Li-Gator Single Use Laparoscopic Clip Applier Recalled by Genicon, Inc....

The Issue: Device malfunction causing the applier to jam, and clip loading failures.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Recalled...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: 9100c NXT system - Product Usage: Device is licensed and Recalled by GE...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: GE Datex-Ohmeda Avance CS2 Anesthesia System - Product Usage: intended...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: GE Datex-Ohmeda Aisys CS2 Anesthesia System - Product Usage: is Recalled by...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· Quidel Corporation

Recalled Item: Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen Recalled by...

The Issue: Instructions for use in the package insert for SARS Antigen FIA test were...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· Getinge Group Logistics America, LLC

Recalled Item: Servo-i Ventilator Recalled by Getinge Group Logistics America, LLC Due to A...

The Issue: A potentially shorter than specified nebulizer connector may result in...

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

Class II — Potential Health HazardOngoing
DrugSeptember 16, 2020· Arbor Pharmaceuticals Inc.

Recalled Item: Nymalize (nimodipine) oral solution Recalled by Arbor Pharmaceuticals Inc....

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugSeptember 16, 2020· Perrigo Company PLC

Recalled Item: Albuterol Sulfate Inhalation Aerosol Recalled by Perrigo Company PLC Due to...

The Issue: Defective Delivery System: Sustained trend of failure to dispense complaints.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 16, 2020· Merit Medical Systems, Inc.

Recalled Item: MeritMedical Cultura Flex Swab Recalled by Merit Medical Systems, Inc. Due...

The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2020· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...

The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2020· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...

The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2020· Boston Scientific Corporation

Recalled Item: Hurricane RX Biliary Balloon Dilatation Catheter Catalog . M00545890...

The Issue: RX tunnel component (black sheath) may detach from the catheter shaft due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2020· 3M Company - Health Care Business

Recalled Item: 3M Red Dot Monitoring Electrode with Foam Tape - Product Recalled by 3M...

The Issue: Corrosion could cause performance failures in the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2020· 3M Company - Health Care Business

Recalled Item: Novaplus Monitoriing Electrode with Foam Tape and Sticky Gel - Recalled by...

The Issue: Corrosion could cause performance failures in the product.

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

Class II — Potential Health HazardOngoing