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. 2,359 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,359 in last 12 months

Showing 4714147160 of 49,744 recalls

Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH ST Product Code: GST61000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx90 GUIDING CATH ST Product Code: GST60900000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
DrugJanuary 10, 2013· Hospira, Inc.

Recalled Item: Furosemide Injection USP (10 mg/mL) Recalled by Hospira, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2013· GE Healthcare, LLC

Recalled Item: Ventri Discovery NM 530c Recalled by GE Healthcare, LLC Due to GE Healthcare...

The Issue: GE Healthcare has recently become aware of an incident which caused a...

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

Class II — Potential Health HazardOngoing
DrugJanuary 8, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: There is the potential for solution to leak...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 8, 2013· Island Delights, Inc.

Recalled Item: Island Delights Almond Chocolate/Almond Mix Natural Flavor Coconut Haystacks...

The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 8, 2013· Island Delights, Inc.

Recalled Item: Island Delights Coconut Haystack Candy Maple Natural Flavor Coconut...

The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 8, 2013· Island Delights, Inc.

Recalled Item: Island Delights COFFEE NATURAL Natural Flavor Coconut Haystacks Recalled by...

The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 8, 2013· Island Delights, Inc.

Recalled Item: Island Delights ALMOND Natural Flavor Coconut Haystacks Recalled by Island...

The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 8, 2013· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 (rev A and Recalled...

The Issue: Neonatal beds and incubator display boards may randomly overwrite stored...

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

Class I — Serious Health HazardOngoing
DrugJanuary 7, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Belladonna Alkaloids (hyoscyamine sulfate Recalled by West-ward...

The Issue: Presence of Foreign Substance: Uncharacteristic blacks spots were found in...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 7, 2013· Somersault Snack Co., LLC

Recalled Item: Somersault brand Cinnamon Crunch. Crunchy nuggets baked with sunflower seeds...

The Issue: During ingredient review for kosher certification, the firm discovered that...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...

The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...

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

Class II — Potential Health HazardOngoing
DrugJanuary 4, 2013· Reumofan Plus USA

Recalled Item: Reumofan Plus Recalled by Reumofan Plus USA Due to Undeclared Active

The Issue: Marketed without an approved NDA/ANDA: Product may contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund