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. 2,489 recalls have been distributed to Mississippi in the last 12 months.
Showing 21841–21860 of 28,172 recalls
Recalled Item: Allofix Insertion Kit Recalled by Musculoskeletal Transplant Foundation,...
The Issue: Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb SofPort Advanced Optics Aspheric Lens Recalled by Bausch &...
The Issue: Haptics breaking during lens loading and insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb SoFlex SE Foldable intraocular Lens Product Usage: Recalled by...
The Issue: Haptics breaking during lens loading and insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿- Solis Ambulatory Infusion Pump Recalled by Smiths Medical ASD, Inc....
The Issue: Smiths Medical has become aware of an issue with an intermittent occurrence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: There exists a possible position sensor fault in the swivel base axis not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Science & Engineering Inc Recalled by American Science &...
The Issue: During factory testing, we discovered that Gemini systems could, in rare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Ambassador Cervical Plate System The Exactech Ambassador Cervical...
The Issue: Shipped to a single consignee prior to completion of final inspection.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Diagnostics Dimension Vista Systems Recalled by Siemens...
The Issue: Two software issues may occur in Vista software version 3.6.1. Issue #1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Single Barrel Drill Guides The Single Barrel Drill Guide Recalled...
The Issue: Shipped to a single consignee prior to completion of final inspection.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra Brachy radiation therapy planning software designed to analyze and...
The Issue: Incorrect dose calculation for Regions of Interest (ROIs) defined on a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte Liquid Bicarbonate Concentrate (Dialysate Concentrate for...
The Issue: Bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...
The Issue: Inadequate curing of adhesive, which may cause the two halves of the spheres...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific G6PD Controls Kit configuration: 6 x 0.5 ml Recalled by...
The Issue: A reduction in the reconstituted stability has been identified. Clinicians...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentraLink" Data Management System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has determined that the sample query function...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaTREK Instrument Series 240 Recalled by Remel Inc Due to Use of the...
The Issue: Use of the recalled product may result in false positive reports.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Tni-Ultra Assay Recalled by Siemens Healthcare Diagnostics,...
The Issue: System-to-system bias between the Tni-Ultra assay on the ADVIA Centaur CP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaTREK Instrument Series 528 Recalled by Remel Inc Due to Use of the...
The Issue: Use of the recalled product may result in false positive reports.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/L Taper with Kinectiv¿ Technology. prosthesis Recalled by Zimmer, Inc. Due...
The Issue: Zimmer is initiating a voluntary recall of 64 lots (752 implants total) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearSight Recalled by Edwards Lifesciences, LLC Due to Edward Lifesciences...
The Issue: Edward Lifesciences is recalling the ClearSight System because the finger...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via and Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: measurements drawn on the 2nd and subsequent images of the series are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.