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. 2,602 recalls have been distributed to Georgia in the last 12 months.
Showing 38661–38680 of 53,623 recalls
Recalled Item: Thin-Flex Venous Cannula Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Edwards Lifesciences initiated a field action for the Thin-Flex Venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bevacizumab 2 mg/0.08 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal...
The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 2.5 mg/0.1 mL in 3/10 mL 31 G 5/16" Recalled by Pine...
The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 1.25 mg/0.05 mL in 3/10 mL 31 G 5/16" Recalled by Pine...
The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 1.25 mg/0.05 mL filled to 0.06 mL in 3/10 Recalled by Pine...
The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT Recalled by...
The Issue: Procedure Products initiated the recall due to the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS V3000 Recalled by Philips Electronics North America Corporation Due...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS CV Recalled by Philips Electronics North America Corporation Due to...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 OR Table Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 15-12 (biplane) Recalled by Philips Electronics North...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 OR Table Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS H5000 Recalled by Philips Electronics North America Corporation Due...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BH3000 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.