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 48,100 notices were distributed nationwide, so they reach Tennessee too — those are in the archive.
Reported Mar 16, 2022
Nature's Eats Balance Hearty Mix 16 oz. UPC 832112003842 packaged in cello bag 5 bags per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Texas Star Nut and Food Co., Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 9, 2022
Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acorn Stairlifts, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioPro, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brasseler USA, Medical LLC
FDA (openFDA device enforcement)
Reported Mar 9, 2022
All Over-The-Counter (OTC) drug products sold by Family Dollar retail stores located in Alabama, Arkansas, Louisiana,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dollar Tree Distribution, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Mar 9, 2022
da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
NavitrackER Kit A: Knee, Model Number 20-8000-000-07,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosoft, Inc. dba Zimmer CAS
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Philips Respironics V60 Ventilator Part Number 1053617
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics California, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Digital Angiography System Bransist safire Generator Model D150GC-40
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2022
Dole 10oz Very Veggie UPC: 0-71430-01008-2 SKU: 532
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
54 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 2, 2022
Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2022
NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nobel Biocare USA LLC
FDA (openFDA device enforcement)
Reported Feb 23, 2022
RNAstill Molecular Transport Medium Vial, Catalog number MTM-001, a component of the following catalog numbers of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Base 10 Genetics Inc.
FDA (openFDA device enforcement)
Reported Feb 23, 2022
Destino Twist 14F (also branded as Guidestar 14F)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oscor Inc.
FDA (openFDA device enforcement)
Reported Feb 23, 2022
Zenition 50, Model #718096
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 16, 2022
1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Feb 16, 2022
ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 16, 2022
Ahold 10oz Chopped Romaine Product UPC 688267011085
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
75 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 16, 2022
Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)- Indicated for long-term (> 6 hours)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Feb 16, 2022
THERAKOS CELLEX Photopheresis Procedural Kit, CLXUSA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mallinckrodt Pharmaceuticals Ireland Ltd.
FDA (openFDA device enforcement)
Reported Feb 9, 2022
CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY, IMMY, Lateral Flow Assay for the Detection of Cryptococcal Antigen in serum…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Immuno-Mycologics, Inc.
FDA (openFDA device enforcement)
Reported Feb 9, 2022
ARIES HSV 1&2 Assay, Catalog/REF# 50-10017
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Feb 9, 2022
KWIK-STIK, Candida parapsilosis derived from ATCC 22019, REF 0726P. Packaged 2 units per pack. IVD controls.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Microbiologics Inc.
2 more products in this recall
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.