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. 2,465 recalls have been distributed to Mississippi in the last 12 months.
Showing 25001–25020 of 28,172 recalls
Recalled Item: Biotene Moisturizing Mouth Spray Recalled by GlaxoSmithKline, LLC. Due to...
The Issue: Label indicates, "Sweetened with xylitol and Sorbitol", however product does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAS I/II Absorbers that are parts of the BleaseSirius Anesthesia Workstation...
The Issue: Spacelabs Healthcare Ltd. of United Kingdom recalls , and Service Kits, Part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 L Cycler Drainage Bag Product Usage: For use with Recalled by Baxter...
The Issue: The large tube clamp used to close the drain tube on the 15 L Cycler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 2 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal" Reverse Shoulder System Recalled by Zimmer, Inc. Due to As...
The Issue: As a result of complaints for disassociation of the TM Reverse Glenosphere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cutera brand truSculpt infrared System (optional) Recalled by Cutera, Inc....
The Issue: Cutera received two adverse events associated with the edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos Recalled by Bausch &...
The Issue: Lens was manufactured with incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The HomeChoice Pro APD System is a peritoneal dialysis system. Recalled by...
The Issue: The occluder in affected devices 1) may have sharp edges that could cut the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to Recalled by...
The Issue: Labeling inconsistency
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer Radiometer Medical ApS Recalled by Radiometer America...
The Issue: RADIOMETER become aware that if the ABL90 FLEX is tilted, this may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Material Mix (Adjustable Cervical Distractor-Right Recalled by...
The Issue: One material batch used for production of the affected parts of the Synthes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva II Recalled by Philips Medical Systems, Inc....
The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty¿ Cycler Part Number: RTLR180111 Product Usage: The Liberty...
The Issue: Fluid leaking may be observed inside the pump compartment of the Liberty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips brand IntelliSpace PACS 4.4 Recalled by Philips Healthcare...
The Issue: Philips Healthcare became aware of a software problem with the IntelliSpace...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva with FlatDetector Recalled by Philips Medical...
The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS TPSA Recalled by BioMerieux SA Due to Product is not approved or...
The Issue: Product is not approved or authorized for distribution in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 14.5 mm Outer Protection Sleeve for Suprapatellar Synthes 14.5...
The Issue: Complaints were received reporting that a product packaged as a 14.5 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epsilon Skin Tensioner:Rx Recalled by Restoration Robotics Due to Reports of...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.