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. 2,489 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,489 in last 12 months

Showing 2084120860 of 49,744 recalls

Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Snap Abutment Engaging CC RP 1.5 mm Recalled by Nobel Biocare Usa...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Abutment Non-Engaging CC RP pre-manufactured prosthetic components...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Snappy Abutment 5.5 CC RP 3 mm Recalled by Nobel Biocare Usa Llc Due to...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Randox Laboratories Ltd.

Recalled Item: Liquid Protein Calibrators (SP CAL (LIQ)) Catalogue Number: IT2691 GTIN:...

The Issue: The assigned value for Rheumatoid Factor over recovers against the material...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Randox Laboratories Ltd.

Recalled Item: Rheumatoid Factor Standard (RF CAL) Catalogue Number: RF2301 GTIN:...

The Issue: The assigned value for Rheumatoid Factor over recovers against the material...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· GE Healthcare, LLC

Recalled Item: Proteus XR/a (SlOK : K993090) Recalled by GE Healthcare, LLC Due to...

The Issue: Intermittently not receiving an audible exposure indication upon completion...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Medline Industries Inc

Recalled Item: Medline SYRINGE Recalled by Medline Industries Inc Due to Samples in the...

The Issue: Samples in the identified lot were found to have incomplete or open...

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2019· Alkermes Inc

Recalled Item: Vivitrol (naltrexone for extended-release injectable suspension) 380...

The Issue: Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2019· Keto Farms LLC

Recalled Item: Keto Farms Keto Snack Mix - Tomato Pepperjack Fruit & Recalled by Keto Farms...

The Issue: California Department of Public Health Inspection found that the allergen,...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2019· Keto Farms LLC

Recalled Item: Keto Farms Keto Snack Mix - Raspberry Gouda Fruit & Recalled by Keto Farms...

The Issue: California Department of Public Health Inspection found that the allergen,...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2019· FIRST START HOLDINGS INC

Recalled Item: Nosh Organic Fruit & Protein Soft Oat Bar Recalled by FIRST START HOLDINGS...

The Issue: Fruit & Protein Soft Oat Bars have the potential to be contaminated with mold.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2019· FIRST START HOLDINGS INC

Recalled Item: Nosh Organic Fruit & Protein Soft Oat Bar Recalled by FIRST START HOLDINGS...

The Issue: Fruit & Protein Soft Oat Bars have the potential to be contaminated with mold.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2019· Keto Farms LLC

Recalled Item: Keto Farms Keto Snack Mix - Strawberry Gouda Recalled by Keto Farms LLC Due...

The Issue: California Department of Public Health Inspection found that the allergen,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2019· BioFire Diagnostics, LLC

Recalled Item: FilmArray Gastronintestinal (GI) Panel Recalled by BioFire Diagnostics, LLC...

The Issue: Complaints have been received concerning elevated rates of false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2019· Radiometer Medical ApS

Recalled Item: AQURE basic sytem Recalled by Radiometer Medical ApS Due to The firm has...

The Issue: The firm has become aware that there is a potential problem relating to the...

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clotrimazole and Betamethasone Dipropionate Cream USP Recalled by Glenmark...

The Issue: Temperature Abuse: Complaints received of liquidy texture.

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing