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 48,122 notices were distributed nationwide, so they reach Tennessee too — those are in the archive.
Reported May 21, 2014
McKesson Radiology-PACS. McKesson Radiology is a medical image and information application that is intended to receive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported May 21, 2014
Syngo Dynamics v9.5 system. A Picture Archiving and Communication System (PACS) intended for acceptance, transfer,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported May 21, 2014
Enaly 1000 BT-12 Ozone Generator, Model # 1000BT-12 The 1000BT-12 ozone generator is capable of delivering up to 1gram…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.William C. Domb, D.M.D., A Professional Corporation
FDA (openFDA device enforcement)
Reported May 14, 2014
Bissinger's Dark Chocolate Bunny Ears, 1 oz, individually wrapped in clear plastic with an ingredient card insert and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Karl Bissinger LLC
FDA (openFDA food enforcement)
Reported May 14, 2014
PRIVATE SELECTION SWEET STRAWBERRY SORBET, Labeled in part: "INGREDIENTS: WATER, SUGAR***DISTRIBUTED BY, THE KROGER…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Co.
FDA (openFDA food enforcement)
Reported May 14, 2014
Mar Cor Purification, Central Water Platform (CWP), 102, 104 and 106. Product Usage: The CWP is a Central reverse…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mar Cor Purification
FDA (openFDA device enforcement)
Reported May 14, 2014
Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize, Deknatel. Indicated for use in soft tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 7, 2014
Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 7, 2014
Phosphatidylcholine Solution for Injection, 50 mg/ mL, 50 mL Vial, Rx Only, Not for Resale. John Hollis Pharmacy, 110…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.John W Hollis Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 30, 2014
The CEP 8 SpectrumGreen (SG) ASR Probe Kit, 20ul (list 06J37-018) is an Analyte Specific Reagent (ASR) containing a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Molecular
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Altasource LLC dba Meta Labs LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device) Catalog Numbers: 1100, 1101, 1102, 1103, 1104,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2014
LifeShield LATEX-FREE HemoSet 100 mL Burette I.V. PlumSet, Nonvented, 105 inch with Prepierced Reseals, OPTION-LOK and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
RaySearch Ray Station Radiation Therapy Treatment Planning System, Stand-alone software. Versions 2.0, 2.5, 3.0, 3.5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Stryker PenAdapt"; Rx Only, Sterile. This device is an accessory to an electrosurgical unit (ESU). The PenAdapt is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Apr 23, 2014
Brainlab, Spine & Trauma 3D 2.0, Navigation Software. An intraoperative image-guided localization system to enable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Apr 23, 2014
Luna Chocolate Chunk; Whole Nutrition Bar for Women; 15 count box. Clif Bar & Company, Emeryville, CA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clif Bar And Company
FDA (openFDA food enforcement)
Reported Apr 23, 2014
VITROS Chemistry Products CRBM Slides, REF 889 2382, IVD -- Ortho-Clinical Diagnostics, Inc. For in vitro diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Apr 16, 2014
7mm Drain Kit, Flat Full Perforated, Saber 100ml Bulb and 3C System Sterile (10/case) Intended for closed wound suction…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aspen Surgical Products, Inc.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 16, 2014
Reusable latex breathing bags with multiple part numbers and sold as part of test lung part number and reusable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 16, 2014
Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Energizer Personal Care
FDA (openFDA device enforcement)
Reported Apr 9, 2014
Integrity 1.1. Integrity is the interface and control software for the Elekta range of medical digital linear…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, 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.