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. 2,476 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,476 in last 12 months

Showing 2358123600 of 49,744 recalls

FoodOctober 15, 2018· Request Foods Incorporated

Recalled Item: Beecher's Mariachi Mac & Cheese 20oz. Frozen 8 Recalled by Request Foods...

The Issue: The firm was notified by their supplier that ingredients used in their...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 15, 2018· Smiths Medical ASD Inc.

Recalled Item: Medfusion¿ Model 4000 Syringe Infusion Pump Recalled by Smiths Medical ASD...

The Issue: Customers who utilize PharmGuard¿ Server Software (PGS) with Medfusion¿ 4000...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...

The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Total T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...

The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Compress Devices and Instruments: Item Number/Item Description 178350...

The Issue: Correction to update the surgical technique for the Compress System. To make...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2018· Atrium Medical Corporation

Recalled Item: Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE Recalled by Atrium Medical...

The Issue: This recall has been initiated in response to a seal defect found in certain...

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

Class II — Potential Health HazardOngoing
DrugOctober 11, 2018· Lannett Company, Inc.

Recalled Item: HydrOXYzine HYDROCHLORIDE SYRUP (HydrOXYzine Hydrochloride Oral Solution...

The Issue: CGMP Deviations: cleaning procedures during manufacturing caused out of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 11, 2018· St. Jude Medical, Inc.

Recalled Item: St. Jude Medical InfinityTM DBS System 8CH Directional Lead Recalled by St....

The Issue: The most proximal unsegmented electrode of the Deep Brain Stimulation leads,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge Recalled...

The Issue: Siemens Healthcare Diagnostics has confirmed that Dimension Vista Lactate...

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

Class II — Potential Health HazardOngoing
FoodOctober 10, 2018· Quest Nutrition, LLC

Recalled Item: Quest Protein Bar Vanilla Almond Crunch Single Bar UPC# - Recalled by Quest...

The Issue: Undeclared allergen; tree nut (almonds)

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 10, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Naera Hospital Bassinet Recalled by Stryker Medical Division of Stryker...

The Issue: It was identified that the volume of air inside the mattress may expand in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Porous Stem Recalled by Zimmer Biomet, Inc....

The Issue: Zimmer Biomet is conducting a lot specific medical device recall for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Zimmer Biomet, Inc.

Recalled Item: Comprehensive Mini Stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet is conducting a lot specific medical device recall for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: A problem has been detected in the Philips IntelliVue MX4O that, if it were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Philips Electronics North America Corp.

Recalled Item: Philips HeartStart FR3 Defibrillator Recalled by Philips Electronics North...

The Issue: Automated external defibrillators may not fully meet IPx5 water ingress...

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

Class II — Potential Health HazardOngoing
DrugOctober 9, 2018· Sprayology

Recalled Item: AllergEase Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: DigestivEase Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: Diet Power Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: MenoPower Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: Woman Power Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund