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.

49,744 total recalls
2,438 in last 12 months

Showing 3492134940 of 49,744 recalls

DrugDecember 15, 2015· Baxter Healthcare Corp.

Recalled Item: Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer compliants of finding an...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Morton Grove Pharmaceuticals, Inc.

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.

Class III — Low RiskOngoing
Refund
FoodDecember 15, 2015· Trader Joes Company

Recalled Item: Triple Ginger Brew Recalled by Trader Joes Company Due to Trader Joes...

The Issue: Trader Joes recalling Triple Ginger Brew due to reports of unopened bottles...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 15, 2015· Mindray DS USA, Inc. dba Mindray North America

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Fresenius Medical Care Renal Therapies Group, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Bio-Rad Laboratories, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2015· Becton, Dickinson and Company, BD Biosciences

Recalled Item: FMC7 FITC Recalled by Becton, Dickinson and Company, BD Biosciences Due to...

The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
DrugDecember 11, 2015· Reesna, Inc

Recalled Item: FUEL UP PLUS Recalled by Reesna, Inc Due to Undeclared Hydroxythiohomosildenafil

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.

Class I — Serious Health HazardOngoing
Refund
DrugDecember 11, 2015· Reesna, Inc

Recalled Item: FUEL UP HIGH OCTANE Recalled by Reesna, Inc Due to Undeclared...

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.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 11, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI¿ H/S Cuvette The intended use for the CDI¿ H Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received complaints of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
FoodDecember 10, 2015· Bulletproof Digital Inc

Recalled Item: FATwater bottle Recalled by Bulletproof Digital Inc Due to Potential E. coli...

The Issue: FATwater bottles, Lemon flavor, are recalled due to microbial growth...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodDecember 10, 2015· Bulletproof Digital Inc

Recalled Item: FATwater bottle Recalled by Bulletproof Digital Inc Due to Potential E. coli...

The Issue: FATwater bottles, Berry flavor, are recalled due to microbial growth...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodDecember 10, 2015· Bulletproof Digital Inc

Recalled Item: FATwater bottle Recalled by Bulletproof Digital Inc Due to Potential E. coli...

The Issue: FATwater bottles, Tangerine flavor, are recalled due to microbial growth...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodDecember 10, 2015· Pine Valley Foods Inc

Recalled Item: Crazy about Cookies 2lb DSC Custom Decorated Sugar Cookies Item Recalled by...

The Issue: Pre-portioned sugar cookie dough contains undeclared milk and pre-portioned...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund