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 48,122 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.
Reported Feb 4, 2015
Thera Tablets with Beta Carotene Dietary Supplement
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Harvard Drug Group, LLC
FDA (openFDA food enforcement)
Reported Feb 4, 2015
Market Pantry Brand Dark Chocolate Covered Almonds 9 oz., UPC 085239555644
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zachary Confections, Inc.
FDA (openFDA food enforcement)
Reported Jan 28, 2015
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2015
PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Testing Institute,Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Liposomal Amphotericin B 130 mg in dextrose bags
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Walgreens Infusion Services
35 more products in this recall
FDA (openFDA drug enforcement)
Reported Jan 21, 2015
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
POWEREASE Instruments Set Screw Breakoff Instrument, REF 2346010, Medtronic Sofamor Danek, USA, Inc. Spinal surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging Cradles are designed to be used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Abdallah Milk Chocolate Bites CARAMEL, Net Wt 4.5 oz. (127g), UPC 7 6668407116 2, Ingredients: Pure milk chocolate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abdallah Candies, Inc.
FDA (openFDA food enforcement)
Reported Jan 14, 2015
McKesson Cardiology ECG Management It is a software application designed to import, display, store, analyze, distribute…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McKesson Israel Ltd.
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Harmony¿ vLED Surgical Lighting System, one unit packaged per box The Harmony¿ vLED Surgical Lighting System is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Cable remote control JUPITER U, Material no.4500119, Serial number: to (incl.) 102306915. Patient positioning during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trumpf Medical Systems, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 7, 2015
J-TAN D PD Drops (bromphenirame maleate 1 mg and pseudoephedrine hcl 7.5 mg/ teaspoon), 1 fl oz (30 mL) Bottle, Over…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jaymac Pharmaceuticals LLC
FDA (openFDA drug enforcement)
Reported Jan 7, 2015
Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safety…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
Bausch & Lomb Stellaris PC w/ Laser, BL14304 The responsible firm name is Bausch & Lomb Incorporated Rochester, NY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 mm, Distributed by Kimberly Clark Global Sales, LLC.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Halyard Health
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
DPM 6 Patient Monitor and DPM 7 Patient Monitor. The product affected is the Mindray IBP module, P/N is 6800-30-50485…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Distal Access Catheter: Model Numbers: 90121, 90130, 90131, 90160. The Distal Access Catheter is intended for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Concentric Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Invacare Perfecto 2 V Oxygen Concentrator The finished device is packaged as a single unit. The service part contains a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Dec 17, 2014
BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT) and integrates with an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Align Radial Stems, Prosthesis, Elbow, Hemi Replacement of the radial head for degenerative or post-traumatic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skeletal Dynamics
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snug Seat Inc.
FDA (openFDA device enforcement)
Reported Dec 10, 2014
MAS CardioImmune XL Cardiac Marker Control; Model: CAI-XL1; intended for use in the clinical laboratory as an assayed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product 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.