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 Jul 16, 2014
Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red & Green Peppers, 19.4 oz 1 LB 3.4 oz), packed in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oregon Freeze Dry, Inc.
FDA (openFDA food enforcement)
Reported Jul 16, 2014
Henora REF: 70-4026-09V1 300psi I.V. Catheter Extension Set Product Usage: Catheter extension set for high pressure…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RGI Medical Manufacturing, Inc.
FDA (openFDA device enforcement)
Reported Jul 16, 2014
The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Dole Garden Soup "Roasted Garlic Tomato Basil", Net Wt. 26 oz. (1lb 10oz) 737 g, UPC 3890002404, 6 units/case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Packaged Foods, LLC
FDA (openFDA food enforcement)
Reported Jul 9, 2014
Stirling Ultracold Portable Shuttle, ULT-25. Storage for cold-chain management, short-term or long-term ultra-low and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Global Cooling Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
MIS Rod 2, a component of the NewPort System. Model No: 60-0545 (45mm); 60-0550 (50mm); 60-0555 (55mm); 60-0560 (60mm);…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Laceration Trays, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc., Arden, NC.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microline Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Manual Resuscitator Bag Series: AF1000, AF2000, AF3000, AF4000, AF5000, BT2000, BT3000, BT4000, BT5000, BVM700,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ventlab LLC
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Glucose Hexokinase Liquid Reagent For the in vitro quantitative determination of Glucose in serum.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JAS Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray System & Brilliance CT Big Bore Radiology Whole…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Integra UCR 3mm Hex, Large Axial Driver. The UCR Hex Axial Driver is a surgical instrument used to implant and remove…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SeaSpine Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Siemens StreamLAB(R) Analytical Workcell; Catalog number 746002.901. Designed to automate sample handling and…
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 Jul 2, 2014
Spacelabs Healthcare Qube Compact Monitor, Model 91390. Intended to alert the user to alarm conditions that are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
ANSPACH***Knotless Suture Anchor Deployment Tool, Custom***Rx Only*** This device is intended to be used with Anspach…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
44 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Western / Scott Fetzer Company
FDA (openFDA device enforcement)
Reported Jul 2, 2014
VerSys¿ Hip System, Beaded Fullcoat Stems, Zimmer, Inc., Warsaw, IN 46581
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jun 25, 2014
Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component of the Puritan Bennett 840 Ventilator:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported Jun 25, 2014
RayStation software version 4.0.3.4 RayStation is a software system designed for treatment planning and analysis of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jun 18, 2014
Horizon Medical Imaging Horizon Medical Imaging is a medical image and information management application that is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
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.