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 7, 2024
Corey B's Oh Baby BBQ Sauce packaged in 12.6oz glass flask - 12 bottles per case
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hoff & Pepper, Co. LLC.
FDA (openFDA food enforcement)
Reported Aug 7, 2024
Arctic Sun Temperature Management Systems, Name/REF: Arctic Sun STAT, NA/6000-00-00; Arctic Sun STAT Loaner,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medivance Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2024
Diamond Shruumz Infused Cones Cookies and Cream UPC 810133320025
High riskUsing this product could cause serious injury, illness or death — stop using it now.Prophet Premium Blends, LLC
21 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 31, 2024
Beckman Coulter, REF: OSR61173, IGM 4x14 mL R1, 4x11 mL R2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jul 31, 2024
ABL800 FLEX Model Numbers 393-800 and 393-801 The ABL800 FLEX analyzers are intended for: " In Vitro testing of samples…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Jul 31, 2024
Sweet Preserved Dried Plums; Farmer's Grange; Series Food; 88g; Plastic synthetic (flexible) package; INGREDIENTS:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tiffany Food Corp.
FDA (openFDA food enforcement)
Reported Jul 24, 2024
Abbott Proclaim XR 5 Implantable Pulse Generator, REF 3660, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2024
Surgical Image Guidance Functionality, software used with NGENUITY 3D Visualization System, Part Number: 8065000399
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
FDA (openFDA device enforcement)
Reported Jul 24, 2024
BD Multitest 6-Color TBNK CE-IVD, REF: 644611; BD Multitest 6-Color TBNK Kit with BD Trucount Tubes CE-IVD, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Jul 24, 2024
VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2024
QIAcube Connect MDx - IVD Instrument designed to perform automated isolation and purification of nucleic acids in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
FDA (openFDA device enforcement)
Reported Jul 24, 2024
Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Jul 24, 2024
Cyanocobalamin Injection, USP, 1,000mcg/mL, 1 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zydus Pharmaceuticals (USA) Inc.
FDA (openFDA drug enforcement)
Reported Jul 17, 2024
C. Kreuger Gluten Free White Chocolate Cherry Oatmeal Cookies, 2oz in plastic sleeve. 60 cookies per case. Storage for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C. Krueger Finest Baked Goods
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 17, 2024
Kosmos on iOS impacting iOS, Model Numbers: P007639, P007944, software is part of a general-purpose diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Echonous Inc.
FDA (openFDA device enforcement)
Reported Jul 17, 2024
Decompression Table Model E9011. This device applies cervical and/or lumbar decompression with practitioner definable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pivotal Health Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2024
AMT Initial Placement Dilator Set. Used to place gastrostomy devices.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Technology Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2024
BD Pyxis, Name/REF: MEDBANK MINI 1FH-1FM/ 169-137, MEDBANK MINI 1FH-2HH MEDPASS/ 169-151, MEDBANK MINI 1HH-1FH-1HM/…
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)
Reported Jul 10, 2024
First Source Vision M. Portable cart and platform that supports an X-ray system and laptop computer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.First Source Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2024
Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX electrophysiology recording system and ComboLab AltiX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Information Technologies Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2024
Sterile surgical convenience kits: a. Medline Cath Lab Special Procedure, Pack #00-RDF0360, containing a Pure Pouch…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2024
Neurostimulation Kit (Ported, Dual 8, 40 cm), REF: 71005-US Peripheral Nerve Stimulation Kit (Ported, Dual 8, 40 cm),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nalu Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2024
Walmart Great Value Organic Black Chia Seeds 32 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Natural Sourcing International,LLC
FDA (openFDA food enforcement)
Reported Jul 10, 2024
Avalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the fetal heart and externally monitors fetal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America 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.