All recall categories

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.

Medical devices

Reported Nov 6, 2013

PIPELINE LS ACCESS SYSTEM, 15 Dilator, 5 mm, Insulated The PIPLINE LS Dilators and Holding Clip are intended for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DePuy Spine, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2013

The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare It

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2013

pocH-100i; sysmex; Automated Hematology Analyzer; 7.3" x 13.8" x 18.1" / 30.8 lbs.; Sysmex Corporation; 1-5-1…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sysmex America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2013

FSE Image Upgrade Kit, Catalog # 92019C This kit is used to install and/or upgrade software used with the EVOLIS…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Bio-Rad Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2013

Synergetics 25 gauge Soft Tip Cannula, packaged in 6 units per box. Catalog number: 30.08.25. Single-use 25 gauge…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synergetics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2013

Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The washer disinfector is used in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Getinge Disinfection

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2013

Brilliance CT Big Bore Oncology, Brilliance CT Big Bore Radiology and Brilliance CT 16 (Air) Brilliance CT Big Bore…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2013

Dimension Vista (R) Urinary/Cerebrospinal Fluid Protein (UCFP) Flex (R) Reagent Cartridge Lot 11349BB The Urinary /…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2013

P21x/5-1 MHz transducer, Part Number P07698-23 Product Usage: The P21x/5-1 MHz phased array transducer is designed for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

SonoSite, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2013

Selenia Full Field Digital Mammography System with software versions 5.0.x and 5.1.x The Selenia Full Field Digital…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2013

Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The intended use is in vitro testing of samples of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

BD Epilor Syringe BD Franklin Lakes, NJ 07417 BD EDC Laagstraat 57, B-9140 Temse-Belgium The Epilor syringe is used in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

SmartSite Low Sorbing Infusion Set, Model#72313E The SmartSite Low Sorbing Infusion Sets are used to administer fluid…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Monaco RTP System Radiation treatment planning

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Invacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

DRI Cocaine Metabolite Assay, labeled as Multigent Cocaine Assay for Abbott Laboratories. 100 ml, IVD Mfg by:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microgenics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Smith Medical, Deltec, REF 21-2386-24, 11 Fr Introducer Set with Peel-Away Sheath, Sterile EO, Rx Only PORT-A-CATH¿ and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Stryker Vision Mounting Arm, for use with other Stryker Endoscopy medical device products for human patients. Model…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Terumo Pall AL6X Arterial Blood Line Filter, labeled in part Terumo Cardiovascular Systems Corporation, packaged as…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6. Intended for use in constructing…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Outlook ES pump is intended for use with B. Braun Medical Inc. Horizon Pump IV Sets. Used to regulate the flow of…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

B Braun Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm (L) Dental Implant Product Usage: Surgical placement in the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet 3i, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 25, 2013

Olde Cape Cod Chipotle Ranch dressing, 16 oz. Item Number: 90997-11630

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cains Foods LP

FDA (openFDA food enforcement)

Medical devices

Reported Sep 25, 2013

Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cincinnati Sub-Zero Products Inc.

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new Tennessee recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Other states

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.