Product Recalls in New York
Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,901 recalls have been distributed to New York in the last 12 months.
Showing 621–640 of 30,153 recalls
Recalled Item: Sperm 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: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Recalled...
The Issue: Labeling contains claims that are not consistently present.
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: 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: 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: Pet Allergy 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: GI Microbiome Profile Small 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: Thyroid TSH 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: Food Intolerance Test Small 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: Food Sensitivity Test Medium 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: Estrogen & Progesterone 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: 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 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 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.
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 Multi-Measurement Module X3. Product Number: 867030. 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 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.