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. 2,372 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,372 in last 12 months

Showing 4464144660 of 49,744 recalls

Medical DeviceAugust 20, 2013· Bio-Rad Laboratories

Recalled Item: FSE Image Upgrade Kit Recalled by Bio-Rad Laboratories Due to The FSE Image...

The Issue: The FSE Image Upgrade kit (part 92019C) is recalled due to issue related to...

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

Class III — Low RiskOngoing
Medical DeviceAugust 19, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHECK FastClix Lancing Device. It is intended for use in Recalled by...

The Issue: Internal Roche inspections have revealed that after the lancet is used for a...

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

Class II — Potential Health HazardOngoing
DrugAugust 16, 2013· Hospira Inc.

Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of assurance of...

The Issue: Lack of assurance of sterility: ineffective crimp on fliptop vials that may...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 16, 2013· Atlantic Pro Nutrients, Inc. dba XYMOGEN

Recalled Item: LipiChol 540 (Omega-3 Phospholipid) Medical Food Dispense by Prescription...

The Issue: Product was labeled as a medical food as opposed to a dietary supplement.

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

Class III — Low RiskOngoing
Refund
FoodAugust 16, 2013· Atlantic Pro Nutrients, Inc. dba XYMOGEN

Recalled Item: XYMOGEN LipiChol (Omega-3 Phospholipid 540 mg) Medical Food Distributed by...

The Issue: Product was labeled as a medical food as opposed to a dietary supplement.

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

Class III — Low RiskOngoing
Refund
FoodAugust 16, 2013· Justin'S Nut Butter

Recalled Item: Chocolate Hazelnut Butter 16oz Jar (Unit Recalled by Justin'S Nut Butter Due...

The Issue: Justin's has initiated a voluntary recall of certain lots of its Maple...

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

Class III — Low RiskOngoing
Refund
FoodAugust 16, 2013· Justin'S Nut Butter

Recalled Item: Maple Almond Butter 16 oz Jar (Unit USPC 894455000322 Recalled by Justin'S...

The Issue: Justi's has initiated a voluntary recall of certain lots of its Maple Almond...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 16, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia S Recalled by Siemens Medical Solutions USA, Inc. Due to The...

The Issue: The detectors on the Symbia S and Symbia T camera systems are supported and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia T Series SPECT + CT Product Usage 1) SPECT: Recalled by Siemens...

The Issue: The detectors on the Symbia S and Symbia T camera systems are supported and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Intact PTH Calibrator (6 pack) Recalled by Siemens Healthcare...

The Issue: PTH Calibrator packaged with only high calibrator.

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

Class III — Low RiskOngoing
Medical DeviceAugust 16, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT Diagnostic imaging system for fixed or mobile Recalled...

The Issue: Issues with the Ingenuity TF PET/CT Software Version 4.0 could pose a risk...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential safety issue involving missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing