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 25541–25560 of 49,744 recalls
Recalled Item: Nuclear Magnetic Resonance Imaging Systems that are indicated for use...
The Issue: When using respiratory gating with Steady Mode ON in Spin Echo sequence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOSEAL Special Applicator Tips in cartons labeled in part Recalled by...
The Issue: Baxter r recalled this device due to the use of an incorrect plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno Recalled by Siemens Medical Solutions USA, Inc Due to During...
The Issue: During manual LAO/RAO rotation at maximum speed or a combination of LAO/RAO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...
The Issue: Resuspension problems: Out of specification for appearance and resuspendability.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile Recalled...
The Issue: Cap may be mislabeled with incorrect part number, although the correct part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope...
The Issue: Under certain circumstances, the firmware makes it possible for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Jow (menthol USP) Pain Gel Recalled by Shadow Holdings DBA Bocchi Labs Due...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave 3 Step Shaving System Recalled by Shadow Holdings DBA Bocchi Labs...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave Post-Shave Moisturizer (salicylic acid) Recalled by Shadow...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave (salicylic acid) Shave Cream Acne Shield Recalled by Shadow...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets USP Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due...
The Issue: Incorrect/Undeclared excipient: Product batches were released into...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baskin Robbins Mint Chocolate Chip Recalled by Dean Foods, Inc. Due to...
The Issue: Product may contain unlabeled coconut.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Allergan Taytulla Softgel Capsules Recalled by Allergan, PLC. Due to...
The Issue: Contraceptive Tablets Out of Sequence.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorting-Drive Product Part Recalled by Beckman Coulter Inc. Due to...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelligent Peri-Analytical Workstation (HW+SW) Recalled by Beckman Coulter...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorting-Drive Professional Part Recalled by Beckman Coulter Inc. Due to...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.