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 Sep 11, 2019
Titan Gel Serum Protein Control: SPE Control Cat. No 5136 1 x 2.0 mL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Helena Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Communications
FDA (openFDA device enforcement)
Reported Sep 4, 2019
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2019
All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Confectionery Arts International, LLC
FDA (openFDA food enforcement)
Reported Sep 4, 2019
Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia Ab
FDA (openFDA device enforcement)
Reported Sep 4, 2019
PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, citric acid, mono and diglycerides of fatty acids, propane…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PreGel America, Inc.
FDA (openFDA food enforcement)
Reported Aug 28, 2019
Kit BD Max Check-Points CPO IVD EU; Catalog # 278102
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
Dole Baby Spinach: 6 oz. (170 g) plastic bag, UPC 0-71430-00964-2, SKU 320; 10 oz. (283 g) clamshell, UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Aug 28, 2019
Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (20 mm) 9630TF20…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
Archer Farms egg salad packaged in 12oz plastic cup with lid, 6 cups per case, refrigerated
High riskUsing this product could cause serious injury, illness or death — stop using it now.Elevation Foods
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 28, 2019
ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 48 oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 21, 2019
BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number: 367001 Product Usage: Blood Alcohol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BIMBO Bakeries USA Inc.
FDA (openFDA food enforcement)
Reported Aug 21, 2019
MED-RX POLYURETHANE FEEDING TUBES: a) 5Fr X 16" (40cm), REF 54-1650R b) 6.5Fr X16" (40cm), REF 54-1665R c) 5Fr X 24"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canadian Hospital Specialties
FDA (openFDA device enforcement)
Reported Aug 21, 2019
iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2019
SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pega Medical Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
The Alinity ci-series System Control Modules which are configured with Alinity c Processing Modules. The Alinity…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Aug 14, 2019
STERILE GRAVES VAGINAL SPECULUM MEDIUM Kit Code # GVS10MST - Product Usage:The speculum is used to spread the walls of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Great Value Mild Taco Seasoning, Net Wt. 1 OZ, Distributed by Wal-Mart Stores, Inc. Bentonville, AR. UPC 0 78742 24572v0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CH Guenther & Sons, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 14, 2019
IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ideal Implant Incorporated
FDA (openFDA device enforcement)
Reported Aug 14, 2019
14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061423 Product Usage: An aid for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
2 more products 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.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.