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. 2,858 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,858 in last 12 months

Showing 24012420 of 29,505 recalls

Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Solution Set with Duo-Vent Spike Recalled by Baxter Healthcare...

The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Clearlink System Solution Set with Duo-Vent Spike Recalled by Baxter...

The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Integrity Implants Inc.

Recalled Item: Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number:...

The Issue: Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...

The Issue: There is an issue with the ventilator battery charger that could lead to an...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Breathe Technologies Recalled by Baxter Healthcare Corporation Due to There...

The Issue: There is an issue with the ventilator battery charger that could lead to an...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...

The Issue: There is an issue with the ventilator battery charger that could lead to an...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...

The Issue: There is an issue with the ventilator battery charger that could lead to an...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2024· New Medical Technologies Gmbh

Recalled Item: Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each) Recalled by...

The Issue: During the assembly of the cartridge to its connecting body part, the valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· New Medical Technologies Gmbh

Recalled Item: Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each) Recalled by...

The Issue: During the assembly of the cartridge to its connecting body part, the valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing