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.
4,233 stored notices name Tennessee, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Tennessee too — those are in the archive.
Reported Aug 28, 2024
ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Inari Medical - Oak Canyon
FDA (openFDA device enforcement)
Reported Aug 28, 2024
IBA Proton Therapy System - PROTEUS 235- Designed to produce and deliver a proton beam for the treatment of patients…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Aug 28, 2024
Great Value; 8oz Apple Juice in 6 pack; 100% Juice; packaged in 8 oz. PET plastic bottles; UPC 0-78742-29655-5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Refresco Beverages US Inc.
FDA (openFDA food enforcement)
Reported Aug 28, 2024
Disposable 5 Lead Cable and Lead Wire System, 50 inches, REF: LW-309DS50/5A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Aug 28, 2024
Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody, REF: 790-4506, IVD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2024
BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics Solution; Catalog (Ref): 444900;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Aug 21, 2024
BioButton REF BIOST06040 with Software version 3.0.20 The BioButton System is a remote monitoring wearable device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biointellisense Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2024
WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Aug 21, 2024
Cepheid, Sample Collection Device, Part: 900-0370
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
FDA (openFDA device enforcement)
Reported Aug 21, 2024
RMU-2000 Automated Chest Compression Device
High riskUsing this product could cause serious injury, illness or death — stop using it now.Defibtech, LLC
FDA (openFDA device enforcement)
Reported Aug 21, 2024
Foppen Smoked Norwegian Salmon Slices - Toast Size, packaged in 8.1oz vacuum foil, packaged within cardboard envelope.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Foppen Paling En Zalm B.V.
FDA (openFDA food enforcement)
Reported Aug 21, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Rapid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
22 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2024
HeartMate 3 System Controllers provided within the following HeartMate 3 Left Ventricular Assist System (LVAS) Implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec LLC
FDA (openFDA device enforcement)
Reported Aug 14, 2024
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Aug 14, 2024
BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2024
Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT 560 VENTILATOR/4096600, PURITAN BENNETT PB560…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
FDA (openFDA device enforcement)
Reported Aug 14, 2024
Frozen Food Processors - Regular Cornbread Muffins packaged in 2oz corrugated cardboard boxes lined with food grade…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Frozen Food Processors, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 14, 2024
TruDi NAV Suction, 0 Degrees; Model/Catalog Number: TDNS000Z. TruDi" NAV Suction Instruments are intended for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 14, 2024
Kenny's Farmhouse Cheese - St. Jerome packaged in plastic vacuum sealed bags in 7oz wedges and whole 15lb wheels
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kenny's Farmhouse Cheese
FDA (openFDA food enforcement)
Reported Aug 14, 2024
Premo King Club Footlong 11.5oz, clear plastic, UPC 612510094259, 4 retail packages per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lipari Foods Operating Company, LLC.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 14, 2024
Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Aug 14, 2024
Panaderia Guatemex - Sheca Redonda packaged in plastic bag
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Panaderia Guatemex
14 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 14, 2024
Wiers Farm - Whole Salad Cucumbers bagged in 2lb plastic bags, 10 bags per carton
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wiers Farm Inc.
26 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 7, 2024
BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, for FILMARRAY Systems, when used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
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.