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. 2,558 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,558 in last 12 months

Showing 1624116260 of 49,744 recalls

Medical DeviceJanuary 28, 2021· Olympus Corporation of the Americas

Recalled Item: Duodenoscope and accessories Recalled by Olympus Corporation of the Americas...

The Issue: Olympus Medical Systems Corporation (OMSC) has received complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2021· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...

The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2021· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...

The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2021· Baxter Healthcare Corporation

Recalled Item: Preventative Maintenance Kits G5010007) and spare part kits (G5064801 and...

The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2021· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...

The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...

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

Class II — Potential Health HazardOngoing
DrugJanuary 27, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP...

The Issue: Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP...

The Issue: Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 27, 2021· Meitheal Pharmaceuticals Inc

Recalled Item: Cisatracurium Besylate Injection Recalled by Meitheal Pharmaceuticals Inc...

The Issue: Labeling: Label mix-up: Carton of Cisatracurium Besylate Injection, USP was...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 27, 2021· Johnson & Johnson Surgical Vision Inc

Recalled Item: TECNIS Toric 1-Piece IOL Recalled by Johnson & Johnson Surgical Vision Inc...

The Issue: Due to the release of nonconforming Intraocular Lenses (IOLs).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Sensis / Sensis Vibe systems with software version VD12 and Recalled by...

The Issue: System may sporadically freeze (lock-up) during operation or while being in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2021· BioFire Diagnostics, LLC

Recalled Item: Gram-Negative Bacteria And Associated Resistance Markers Recalled by BioFire...

The Issue: The firm has identified an increased risk of false positive Pseudomonas...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2021· BioFire Diagnostics, LLC

Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to The firm has...

The Issue: The firm has identified an increased risk of false positive Pseudomonas...

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

Class II — Potential Health HazardOngoing
DrugJanuary 25, 2021· Nostrum Laboratories Inc

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 25, 2021· Goodman Food Products Texas Inc

Recalled Item: O Organics Plant Based Mushroom and Veggie Organic Burger Patties Recalled...

The Issue: Labeling error caused product to claim Gluten Free and Vegan when it...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 25, 2021· Wildtree Inc.

Recalled Item: "Wildtree***Leslies Chili Blend***Organic & Gluten Free***Net Wt. 3.7 oz....

The Issue: Spice mixes contain undeclared gluten due to contaminated ingredient.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 25, 2021· Wildtree Inc.

Recalled Item: "Wildtree***Taco Seasoning***Organic & Gluten Free***Net Wt. 8...

The Issue: Spice mixes contain undeclared gluten due to contaminated ingredient.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 25, 2021· Corin Ltd

Recalled Item: Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 Recalled by Corin Ltd...

The Issue: The size indicated on the labeling on the outer packaging, on the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2021· Corin Ltd

Recalled Item: Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Recalled by Corin...

The Issue: The size indicated on the labeling on the outer packaging, on the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2021· Medline Industries Inc

Recalled Item: RNA MEDICAL Recalled by Medline Industries Inc Due to Product was...

The Issue: Product was compromised during shipment.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2021· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Digitial Medica X-ray Imagining System Recalled by Shanghai United Imaging...

The Issue: There is a potential for the X-Ray tube head (Touch screen interface) to...

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

Class II — Potential Health HazardOngoing