Product Recalls in Colorado
Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,724 recalls have been distributed to Colorado in the last 12 months.
Showing 621–640 of 28,964 recalls
Recalled Item: Melatonin 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: Neurotransmitters XL 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: Pollen Allergy 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: Neurotransmitters Plus 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: 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: Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" Recalled by...
The Issue: Labeling contains claims that are not consistently present.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parasite 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: HPV Antigen 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 HbA1c 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: 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: MPOX 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: Cholesterol 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: IBS Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution without...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Candida 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: 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 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.
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: Olympus OER-Elite 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: Lumify Diagnostic Ultrasound System models : 795005 Recalled by Philips...
The Issue: Ultrasound system compatibility issues with Apple devices running iOS 18 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX500. Product Number: 866064. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.