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 48,122 notices were distributed nationwide, so they reach Tennessee too — those are in the archive.

Medical devices

Reported Aug 3, 2016

Syva¿ EMIT¿ 2000 Theophylline - Catalog # 4P019UL /SMN#10445324 is a homogeneous enzyme immunoassay intended for use in…

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)

Medical devices

Reported Aug 3, 2016

AUTOCOMP6 XPS High Speed Compounder REF 58810

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

The Metrix Company

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

AMD-RITMED brand Conforming Stretch Gauze Bandages, Sterile, 6 in x 4/1 yds./15 cm x 3.7 cm, Reorder Number/Code D606,…

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

Amd-Ritmed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz.

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

Amerx Health Care Corp.

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Frozen Organic Premium Sweet Baby Peas, Organic by Nature brand, net wt. 5 lb. The UPC is 8 46358 00063 3. Frozen IQF…

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

CRF Frozen Foods, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS), Device Listing No.: D017878 is an in vitro diagnostic test…

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

CSL Behring GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

DeVilbiss Model 7305P-D Powered Suction Unit

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

DeVilbiss Healthcare LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Kellogg's Special K Mini Brownies Blondie, 6 ct, 4.44 oz.

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

Kellogg Company

24 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

Parker Trach-Vac Endotracheal Tubes. Tyvek pouches, 10 per box. Product Usage: The product is an endotracheal tube with…

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

Parker Medical

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Tosi Cappuccino Crunch Almond SuperBites, 12 bars per pack, Net Wt. 2.6 ounces, UPC 755918046106

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

Simple Health LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part…

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

HX2" Temperature Management Systems; The Terumo¿ HX2" Temperature Management System provides temperature control of two…

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

Terumo Cardiovascular Systems Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper…

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

WalkMed Infusion, LLC

16 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

Femoral Arterial Line Catheterization Kit with Sharps Safety Features 510K 810675, product code DQX, Device Listing…

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

Arrow International Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009 & MST0815. Each disposable probe is packaged…

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

Devicor Medical Products Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

HeartWare Ventricular Assist System: HeartWare Battery, Lithium Ion, 14.8 V, Rx only. Catalog 1650 (US) and 1650,…

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

Heartware, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…

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

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

AORTIC ARCH CANNULA, Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass (part numbers NA-55X7 and NA-55X8)…

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

Sorin Group USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…

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

Synthes (USA) Products LLC

17 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 20, 2016

Kroger SALAD TOPPERS Roasted & Salted Sunflower Kernels NET WT 3.5 OZ (99G) INGREDIENTS: SUNFLOWER KERNELS, COTTONSEED…

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

The Kroger Co.

1 more product in this recall

FDA (openFDA food enforcement)

Meat & poultry

Reported Jul 14, 2016

U.S. Cado Holdings, Inc. Recalls Imported Siluriformes Fish Products Distributed Without Meeting FSIS Requirements

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

U.S. Cado Holdings, Inc.

USDA FSIS

Medical devices

Reported Jul 13, 2016

ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER. Product Usage: Indicated to…

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

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2016

Covidien Cytosponge Cell Collection Kit. Contains Cytosponge Cell Collection Device, Specimen Jar with preservative.…

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

Covidien, LLC

1 more product in this recall

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.