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. 2,859 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,859 in last 12 months

Showing 761780 of 29,505 recalls

Medical DeviceOctober 7, 2025· Philips Respironics, Inc.

Recalled Item: SimplyGo Mini Recalled by Philips Respironics, Inc. Due to Certain serial...

The Issue: Certain serial numbers of the SimplyGo Mini standard battery kit contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2025· NeuroLogica Corporation

Recalled Item: GM85 Digital Mobile X-ray imaging System Recalled by NeuroLogica Corporation...

The Issue: The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2025· Trividia Health, Inc.

Recalled Item: Good Neighbor Pharmacy Recalled by Trividia Health, Inc. Due to...

The Issue: Manufacturing defect causing LCD display issues with missing or partial...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC

Recalled Item: OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control...

The Issue: A labeling error was identified on the affected product. The expiration date...

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

Class III — Low RiskOngoing
Medical DeviceOctober 6, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Food Panel 3 Specific Allergen Recalled by Siemens Healthcare Diagnostics,...

The Issue: The barcode orientation on affected devices causes incorrect scanning order...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400...

The Issue: Sterility compromised from small holes that may occur during packaging of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: 3gAllergy Specific IgE Universal Kit Recalled by Siemens Healthcare...

The Issue: The barcode orientation on affected devices causes incorrect scanning order...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Oak Mix Specific Allergen Recalled by Siemens Healthcare...

The Issue: The barcode orientation on affected devices causes incorrect scanning order...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name:...

The Issue: Sterility compromised from small holes that may occur during packaging of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Tandem Diabetes Care, Inc.

Recalled Item: Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are...

The Issue: Insulin pump includes a vibration motor that gives tactile feedback for any...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2025· Medtronic Perfusion Systems

Recalled Item: MC3 VitalFlow Console Recalled by Medtronic Perfusion Systems Due to As of...

The Issue: As of August 6, 2025, Medtronic has received eleven reports of VitalFlow...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: TruDi¿ Navigation System - Multi Instrument Adapter Recalled by Integra...

The Issue: It was determined that when the navigation system is configured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model...

The Issue: The motorized longitudinal movement of the FlexArm stand may be inconsistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2025· Cerenovus Inc

Recalled Item: CEREPAK Detachable Coil System - Name/ 2MM X 2.5 CM/FCX100202 Recalled by...

The Issue: Detachable coils system may fail to detach, which could result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 2, 2025· ICU Medical, Inc.

Recalled Item: IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave Recalled by...

The Issue: IV Gravity burette administration set burette component is missing an...

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

Class I — Serious Health HazardOngoing