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.
Showing 621–640 of 29,505 recalls
Recalled Item: Adrenal Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Organic Acids Profile Test Large Recalled by GET TESTED INTERNATIONAL AB Due...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urinary Tract Infection Test Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DHEA Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diabetes Test (ketones & glucose) Recalled by GET TESTED INTERNATIONAL AB...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcohol (ALC) Test Saliva Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iodine Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ovulation Test (5 tests) Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allergy Test IgE Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software...
The Issue: A software timing and processor communication issue in MiniMed" 780G...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX850. Product Number: 866470. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP2. Product Number: M8102A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX700. Product Number: 865241. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus OER-Pro Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...
The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX600. Product Number: 865242. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP5. Product Number: M8105A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP60. Product Number: M8005A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP20. Product Number: M8001A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP80. Product Number: M8008A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP50. Product Number: M8004A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.