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 Aug 30, 2017
Medium Coated Jo-Jo Wedges / 00040 (5lb bags)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Penobscot McCrum LLC
9 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 23, 2017
Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 23, 2017
VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Plum 360 Infusion System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 16, 2017
Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.International Medsurg Connection, Inc.
58 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Aug 2, 2017
STOCKERT Heater-Cooler System 3T, 230 V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2017
Agfa Healthcare NX 3.0.8950 Imaging Processing Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jul 26, 2017
MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CryoLife, Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Simple truth Dry Roasted Macadamia Nuts 12 oz bags UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Corporate Food Technology Laboratory
FDA (openFDA food enforcement)
Reported Jul 19, 2017
The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Chili Pequino 0.25 oz packaged in a clear plastic bag; Product Code 10106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bolner's Fiesta Products, Inc.
FDA (openFDA food enforcement)
Reported Jul 12, 2017
Electrophysiology catheter cables are designed as electrode cables with a multi-pin connector on the distal end and the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sterilmed Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2017
Pointe Scientific CRP(HS) Wide Range Control Set and Pointe Scientific CRP(HS) Wide Range Standard Set 5 Levels of 1 x…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medtest Holdings, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 5, 2017
Kroger Dessert Cups yellow sponge cakes NET WT 6.5 oz (184g) INGREDIENTS: ***NONFAT M ILK***CONTAINS: WHEAT, EGGS, SOY.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
FDA (openFDA food enforcement)
Reported Jun 28, 2017
PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Monfitello
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 28, 2017
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Adenovirus (20/11 & 2/6); 0.5 mL Catalog # 212M-15; and 7.0 mL Catalog number 212M-18 Microbiology - Analyte Specific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cell Marque Corporation
11 more products in this recall
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.