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Recalls distributed in Mississippi

These notices name Mississippi in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

2,477 stored notices name Mississippi, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.

Medical devices

Reported Apr 19, 2023

Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a next generation, self-contained hemodialysis system…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Outset Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 12, 2023

Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath, 8.5F(Small), REF D-1385-01-S, RX CE 2797, Sterile

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biosense Webster, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 12, 2023

Astor Chocolate Wafer Stick NWT WT. 11.64 OZ 330g UPC 72375102886

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Eastland Food Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Apr 12, 2023

Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed REF 86051 7.0 mm I.D. The Shiley Lo-Pro Oral/Nasal Tracheal Tube…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

Instructions for Use for the following Leksell Stereotactic System and Leksell Neurosurgical Instruments: (1) Part…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta Instrument AB

FDA (openFDA device enforcement)

Food

Reported Apr 5, 2023

Rold Gold Original Classic Tiny Twists Pretzels in 16oz UPC 2840004768 packaged in a flexible bag

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Frito-Lay, Inc. Headquarters

FDA (openFDA food enforcement)

Medical devices

Reported Apr 5, 2023

Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Mar 29, 2023

BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 29, 2023

DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Dollar General Corporation

FDA (openFDA food enforcement)

Food

Reported Mar 29, 2023

Russel Stover Sugar Free Peanut Butter Cups packaged in 2.4oz peg bag, containing individually wrapped pieces. UPC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Russell Stover Candies Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 22, 2023

Egg roll wrappers, 6" x 6" and 7" x 7", packaged in 30lb. corrugated (cardboard) boxes. Product is sold frozen.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Baily International Foods

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 22, 2023

Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 22, 2023

Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Brainlab AG

FDA (openFDA device enforcement)

Food

Reported Mar 22, 2023

Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Keurig Dr Pepper

FDA (openFDA food enforcement)

Food

Reported Mar 22, 2023

ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Mead Johnson & Company

FDA (openFDA food enforcement)

Medical devices

Reported Mar 22, 2023

TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 200MM STERILE. Intended for temporary fixation and stabilization of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synthes (USA) Products LLC

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Mar 22, 2023

Colchicine Tablets, USP 0.6 mg, Rx Only, a) 30 tablets per bottle, NDC 16714-0039-01, b) 100 tablets per bottle, NDC…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Zydus Pharmaceuticals (USA) Inc.

FDA (openFDA drug enforcement)

Food

Reported Mar 15, 2023

Given Imaging SmartBar Cereal Bar; Net Weight 2.53 oz (72 g); Ingredients: glucose syrup, soy crisps, oats, pea…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Given Imaging Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 15, 2023

PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Preat Corp.

FDA (openFDA device enforcement)

Food

Reported Mar 8, 2023

HEILEMANN CONFISERIE WEHNACHTSFIGUREN AUS EDELVOLLMILCH-SCHOKOLADE Solid Chocolate Holiday Treats 3.5 oz box UPC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alpenland International, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 8, 2023

Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2023

iTotal Identity Impactor Handle, Model No. 1080-212/ED-07827 REV AE

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Conformis, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2023

The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.