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. 2,535 recalls have been distributed to Mississippi in the last 12 months.
Showing 19261–19280 of 49,744 recalls
Recalled Item: Morrison's cornbread dressing packaged in 7lb trays Recalled by Savannah...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Morrison's cornbread dressing packaged in 4lb tray Recalled by Savannah Food...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Piccadilly Cornbread Dressing in 2# trays Recalled by Savannah Food Company,...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Savannah Classics Classic Cornbread Dressing packaged in 7lb trays Recalled...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Savannah Classics Special Cornbread Dressing packaged in 7lb trays Recalled...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Integris Allura 9 Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardio Vascular-Allura Centron Recalled by Philips North America, LLC Due to...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroDiagnost Eleva Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniDiagnost Eleva System codes 708028 708027 Recalled by Philips North...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integris Allura 15 & 12 Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Poly G Integris H5000 Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura CV20 Recalled by Philips North America, LLC Due to A capacitor inside...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Exper FD Series. System codes 722003 722010 722022 722005 Recalled by...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: Recalled by Smith &...
The Issue: Due to a potential for sterile barrier breach. A complaint was received that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dawson-Mueller Drainage Catheter Recalled by Cook Inc. Due to Specific lots...
The Issue: Specific lots of the Dawson-Mueller Drainage Catheter were not manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proparacaine Hydrochloride Ophthalmic Solution Recalled by Akorn, Inc. Due...
The Issue: Chemical contamination; out of specification results obtained for equipment...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blisovi Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets USP...
The Issue: Failed Tablet/Capsule Specifications: Complaints related to crumbling of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prometra II 20mL Pump. Catalog No. 13827 The device is Recalled by Flowonix...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmable 20mL Pump. Catalog No. 91827 The device is Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.