Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,460 recalls have been distributed to Mississippi in the last 12 months.
Showing 25781–25800 of 49,744 recalls
Recalled Item: ARTIS Pheno Interventional Fluoroscopic X-Ray System Recalled by Siemens...
The Issue: If the C-arm is manually moved in the longitudinal direction to a fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to After the...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic Recalled by...
The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee MP Recalled by Siemens Medical Solutions USA, Inc Due to After the...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniDiagnost Classic X-ray system Angiographic and Diagnostic Recalled by...
The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen biplane Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor MN Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Bronchial Cytology Brushes Recalled by Hobbs Medical, Inc. Due to...
The Issue: Device was marketed for uses outside the 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Docetaxel injection concentrate Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Superpotent drug: over-concentrated vials of Docetaxel injection concentrate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Revolution EVO Recalled by GE Healthcare Japan Corporation Due...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. The systems are intended for head Recalled by GE...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. Sold under the following product names: Recalled...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.