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.
2,512 stored notices name Mississippi, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.
Reported Oct 30, 2019
Tuna salad under the following brand names: BALLARDS FARM Barboursville, WV 25504 UPC 076010000293 12 oz. plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mrs. Stratton's Salads, Inc.
FDA (openFDA food enforcement)
Reported Oct 30, 2019
GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 23, 2019
Nana's Been a Nut Bread NET WT. 11oz/311.74g cloth bag CONTAINS WHEAT AND SOY. MADE ON EQUIPMENT THAT MAKES PRODUCTS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gullah Gourmet, Inc.
FDA (openFDA food enforcement)
Reported Oct 23, 2019
Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical Inc.
21 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 23, 2019
Pantoprazole Sodium Delayed Release Tablets, USP, 40 mg, packaged in 90-count bottle, Rx only, Manufactured by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jubilant Cadista Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Oct 16, 2019
BioEnvelope, surgical mesh envelope. Labeled as the following: 1. BioEnvelope (Medium) (single pack); 2. BioEnvelope…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aziyo Biologics
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
AIR Technology Anterior Array, Catalogue Numbers: (a) 5746694, (b) 5746695, (c) 5746696, a receive-only RF coil…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
Clinical Chemistry, ABX Pentra Lipase CP, ABX Pentra 400/Pentrac400, REF: A11A01631, Model/Part # 1220001631, UDI #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horiba Instruments Incorporated
FDA (openFDA device enforcement)
Reported Oct 16, 2019
Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190 Analyzer/Module: cobas c 311 and cobas c 501/502
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 9, 2019
TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog # 5541-A-201 - Product Usage: Triathlon Femoral Distal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 9, 2019
SE Grocers **BAKERY** 18 CT Peanut Butter Cookies
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Southeastern Grocers - Marketi
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 2, 2019
Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GN Otometrics
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Medfusion¿ Model 4000 Syringe Infusion Pump, with PharmGuard¿ Server Software (PGS). Sold under the following names:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2019
Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2019
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2019
Ore Ida Spud Bites, packaged in 5lb. plain poly foodservice bags, six bags per case, frozen, Case UPC: 1 00 72714 00093…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McCain Foods USA
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Allergan PLC
14 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2019
YoCrunch VANILLA LOWFAT YOGURT WITH SNICKERS PIECES 4 - 4 oz (113g) - 16 oz (453g) 6 packaged or 4 cups per case. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Danone Waters
FDA (openFDA food enforcement)
Reported Sep 18, 2019
PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2019
XP- CR Tibial Tray- Interlok 59mm Item # 195268
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
34 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2019
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2019
PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, citric acid, mono and diglycerides of fatty acids, propane…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PreGel America, Inc.
FDA (openFDA food 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.