Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,472 recalls have been distributed to District of Columbia in the last 12 months.
Showing 23681–23700 of 47,654 recalls
Recalled Item: Skin Irritation & Itch Response Homeopathic Formula Recalled by Beaumont...
The Issue: CGMP Deviations: products manufactured by contract manufacturer under...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diarrhea Response Homeopathic Formula Recalled by Beaumont Bio-med, Inc. Due...
The Issue: CGMP Deviations: products manufactured by contract manufacturer under...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy & Hay Fever Relief Homeopathic Formula Recalled by Beaumont Bio-med,...
The Issue: CGMP Deviations: products manufactured by contract manufacturer under...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sinus Response Homeopathic Formula Recalled by Beaumont Bio-med, Inc. Due to...
The Issue: CGMP Deviations: products manufactured by contract manufacturer under...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colds & Flu Response Homeopathic Formula Recalled by Beaumont Bio-med, Inc....
The Issue: CGMP Deviations: products manufactured by contract manufacturer under...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arthritis Pain Relief Homeopathic Formula Recalled by Beaumont Bio-med, Inc....
The Issue: CGMP Deviations: products manufactured by contract manufacturer under...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Muscle & Joint Pain Relief Homeopathic Formula Recalled by Beaumont Bio-med,...
The Issue: CGMP Deviations: products manufactured by contract manufacturer under...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sore Throat & Laryngitis Response Homeopathic Formula Recalled by Beaumont...
The Issue: CGMP Deviations: products manufactured by contract manufacturer under...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dash 5000 Patient Monitoring System is used to monitor physiologic Recalled...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solar 9500 Information Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solar 8000M Patient Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dash 3000 Patient Monitoring System is used to monitor physiologic Recalled...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dash 4000 Patient Monitoring System is used to monitor physiologic Recalled...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solar 8000i Patient Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuoSaph Plus Endoscopic Vessel Harvesting System Recalled by Terumo...
The Issue: The system's IFU contains a list of generators that the have been deemed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ashland(TM) Box Film Ball Cube II EBT3 Recalled by Accuray Incorporated Due...
The Issue: the Ball Cube II phantom calibration film was not manufactured within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB + Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...
The Issue: The product was shipped after its expiry date due to a system error. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.