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. 2,573 recalls have been distributed to Mississippi in the last 12 months.
Showing 14381–14400 of 49,744 recalls
Recalled Item: Lightly Salted Cashew Halves & Pieces Recalled by Suntree Snack Foods, LLC...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salted Cashews Halves & Pieces Recalled by Suntree Snack Foods, LLC Due to A...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lightly Salted Cashews Halves & Pieces Recalled by Suntree Snack Foods, LLC...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roasted Lightly Salted Cashew Halves and Pieces Recalled by Suntree Snack...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 100 Calorie Packs Lightly Salted Roasted Cashews Halves & Pieces Recalled by...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) Recalled...
The Issue: 3D-RA is a reconstruction software product that can be used with the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Permobil TiLite Recalled by TiSport, Llc Due to Some affected wheelchairs,...
The Issue: Some affected wheelchairs, with transit tie downs, that are used as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-Ray System Recalled by Philips...
The Issue: When the user presses or releases both the APC (accept) button and the Float...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software error, the software can produce an incorrect interpretation of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Packaged dental implant contains a different size then the size declared on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Packaged dental implant contains a different size then the size declared on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinician Programmer Application (CPA) model A610 Clinician Software...
The Issue: A software anomaly may occur with the clinician programmer application.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIMPLEXA COVID-19 Positive Control Pack Recalled by DiaSorin Molecular LLC...
The Issue: Due to unapproved raw materials used in the manufacturing of Covid-19...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Testosterone Propionate Recalled by New Vitalis...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RayStation/RayPlan versions 4 - 11A Recalled by RAYSEARCH LABORATORIES AB...
The Issue: An issue where the combined density in a dose grid voxel partially covered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.