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 Aug 4, 2021
CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperVision Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Del Monte Fresh Cut Golden Sweet Whole Kernel Corn; 15.25 oz. can (24 x 15.25 oz. cans per case) Case UPC …
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 4, 2021
OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Proteus 235-Proton Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Backcountry Dried Apricots 9ounce plastic bag 12 packages per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC.
FDA (openFDA food enforcement)
Reported Aug 4, 2021
basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Used to inflate and deflate an angioplasty balloon or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Now Real Food Organic Steel Cut Oats, 2 lb bag, code 6295, UPC 733739062956, packed 8 bags per case; case packaging is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NOW Health Group Inc.
FDA (openFDA food enforcement)
Reported Aug 4, 2021
RANDALL GREAT NORTHERN BEANS 48OZ glass jar UPC 070095000100; RANDALL GREAT NORTHERN BEANS 24OZ glass jar UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randall Foods, Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 4, 2021
RayStation (Radiation Treatment Planning System) : RayStation 9A, 9B, 9B SP1, 10A, 10A SP1, 10B and 11A, in combination…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Aug 4, 2021
ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sunrise Medical (US) LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Suture Anchor, BioComposite SwiveLock C, 5.5 mm x 19.1 mm, Closed Eyelet, REF AR-2323BCC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Kroger brand, Vitamin D3 125 mcg softgels, 100 count, Green HDPE packaging
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bountiful Trading Inc.
FDA (openFDA food enforcement)
Reported Jul 28, 2021
Infant Heel Warmer with Attachment Tab, Nonsterile, Active Product SKU MH00002T The infant heel warmer is activated at…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Extra Large Premium Cotton Ovals - two textures soft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Jul 28, 2021
NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for measurement of NEFA Catalog Number: FA115
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an…
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 Jul 24, 2021
Top Notch Jerky LLC. Recalls Beef Jerky Products Due to Misbranding and Undeclared Allergens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Top Notch Jerky LLC.
USDA FSIS
Reported Jul 21, 2021
Toshiba Vantage Tiitan 1.5T with Standard gradient, Premium Open-Bore MRI System, REF: MRT-1504 - Product Usage: use as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 21, 2021
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Jul 21, 2021
Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 21, 2021
Hang&Go (kit for hyperthermic perfusion), Reference Code R9900120
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RanD S.r.l.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
Beech-Nut brand Single Grain Rice Baby Cereal; NET WT. 8 OZ (227g); INGREDIENTS: Rice flour, sunflower lecithin;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beechnut Nutrition
FDA (openFDA food enforcement)
Reported Jul 14, 2021
FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product 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.