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. 2,438 recalls have been distributed to Mississippi in the last 12 months.
Showing 34901–34920 of 49,744 recalls
Recalled Item: Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by...
The Issue: Dove Chocolate Assortment Snowflakes may contain undeclared peanuts, what...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by Bio-pharm, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Product recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VP-CH-PNV PRENATAL/POSTNATAL Prescription Folic Acid-Containing Dietary...
The Issue: Defective Delivery System: Product may contain leaking capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardiosave Hybrid and rescue IABP Recalled by Maquet Datascope Corp -...
The Issue: Maquet has recieved information that in some Cardiosave IABPS, the scroll...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF Recalled by Stryker...
The Issue: There were two potential interference conditions identified with the way the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...
The Issue: An issue with the Panorama Central Station may cause the system to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...
The Issue: The door latch may not fully close and the door may open unexpectedly. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...
The Issue: On a rare occasion, there is a potential to assign a patient result to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XCEL ADVANCED Capsules Recalled by Bee Extremely Amazed LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EVOLVE BEE POLLEN Capsules Recalled by Bee Extremely Amazed LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XCEL Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared Fluoxetine
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: La' Trim Plus Capsules Recalled by Bee Extremely Amazed LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asset extreme+PLUS Capsules Recalled by Bee Extremely Amazed LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lindane Lotion Recalled by Morton Grove Pharmaceuticals, Inc. Due to...
The Issue: Super-Potent Drug: Out of Specification Assay test results were reported for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.