Recalls distributed in Tennessee
These notices name Tennessee 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.
4,181 stored notices name Tennessee, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,124 notices were distributed nationwide, so they reach Tennessee too — those are in the archive.
Reported Aug 28, 2013
Moore Hip Prosthesis Long Fenestrated Stem, several head Diameter, 203 mm Stem length. Used to seat the prosthesis with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
47 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2013
epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing of samples for pH, pCO2, pO2, Sodium…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epocal
FDA (openFDA device enforcement)
Reported Aug 21, 2013
GE LightSpeed CT750 HD The GE LightSpeed CT750 HD Computed Tomography X-ray system is intended to produce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2013
Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375, 2) 6801890, 3) 6802445, 4) 6802413 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Aug 21, 2013
3.2mm Drill Bit. This is a component within the PediLoc Locking Plate System utilized to pre-drill a hole in bone prior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Aug 21, 2013
ADVIA Centaur Calibrator A. Cat. #04800735, SMN 10285904 (6 pack); Cat. # 04800840, SMN 10285905 (6 pack - REF). For…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2013
Siemens AXIOM Artis zeego x-ray, angiographic system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Vena Cava Filter and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cordis Corporation
FDA (openFDA device enforcement)
Reported Aug 14, 2013
MRidium 1145 Dose Reduction System (DERS) drug library kit. (This is an option for the MRidium 3860+MR Infusion Pump…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Iradimed Corporation
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Medtronic Mullins Transseptal Adult 7F, REF 008551. Intended for the introduction of cardiovascular catheters into the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Nestle Nutrition, Compat, Enteral Feeding Tube, sterile, 8 French (REF 08310400), 10 French (REF 08310600), and 12…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle HealthCare Nutrition
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Non-sterile Viscot Surgical Skin Markers Part Number 1437-100 Non-sterile Viscot Part Number 143-100 Surgical Skin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Precision Dynamics Corporation
FDA (openFDA device enforcement)
Reported Aug 14, 2013
TCM4 series Base Units, and spare part Power Supply, Radiometer Medical ApS, Akandevej 21, Br¿nsh¿j, Denmark,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL (DC107) Product Usage: The TACR method is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2013
ADVIA Centaur Systems TSH3 Ultra ReadyPack ((REF 06491072 - 100 Tests, REF 06491080 - 500 Tests, REF 04862625 - 2500T).…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2013
R3 (TM) XLPE ACETABULAR LINER UHMWPE, 20o OVERHANG, 36 MM ID, 62 MM OD, QTY: (1), STERILE H2O2, REF 71335762.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Raw Pistachio Halves, 1 pound bag. Item Number 11910, UPC Code: 172043119107; Raw Pistachio Halves, 4 pound bag. Item…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Superior Nut Co. Inc.
FDA (openFDA food enforcement)
Reported Aug 7, 2013
LPS Lower Extremity Dovetail Intercalary component. Intended for use in replacement of the mid-shaft portion of the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
GE Healthcare, VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM. The device is a general purpose ultrasound…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 7, 2013
Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
OSKRI, Coconut Bar Dark Chocolate, Net Wt. 1.9 oz ( 53g), UPC 6 66016 30070 3. Ingredients: Coconuts 55%, Rice Syrup,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oskri Corp.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 7, 2013
Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Picis Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
GAMMA3 System Long Nail Kit, R2.0, Ti, Left Distributed in USA by Howmedica Osteonics Corp., 325 Corporate Drive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
Synthes Large External Fixation, MR Conditional, Tube to Tube Clamp, Part Number 390.007, Lot Number 6800599 Synthes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
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.