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 Jul 3, 2024
2nd Generation CentriMag Primary Console, REF: 201-90401, 201-90701, 201-90411, 201-90421, 201-30300, L201-90401,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Switzerland GmbH
FDA (openFDA device enforcement)
Reported Jun 19, 2024
MRI systems: Vantage Orian MRT-1550 (MEXL-1550), Vantage Elan MRT-2020 (MEXL-1520), Vantage Titan MRT-1504 (MEXL-1504),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2024
EsoFLIP, 30mm BALLOON DILATION CATHETER, REF ES-330, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LLC
FDA (openFDA device enforcement)
Reported Jun 19, 2024
MyoSPECT System, Model H3912AA and H3912B, and MyoSPECT ES System, Model H3912AB and H3912BD, dedicated cardiac SPECT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ge Medical Systems Israel, Functional Imaging
FDA (openFDA device enforcement)
Reported Jun 19, 2024
Grande Lactose SKU 30600. Grade A. Refined Pasteurized. Net Wt 25 kg. Ingredients: Lactose Contains Milk. Grande Custom…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grande Cheese Company
10 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 19, 2024
VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs Calibrator Pack contains 3 X labelled…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2024
Darby Prophylaxis Paste with 1.23% Fluoride Ion, Mint Coarse
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Young Dental Manufacturing I, LLC
FDA (openFDA device enforcement)
Reported Jun 12, 2024
ADVANTA VXT, 5X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
67 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Germantown Stabilizer 1772-II, Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
High riskUsing this product could cause serious injury, illness or death — stop using it now.Danisco USA Inc.
35 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 12, 2024
FSIS Issues Public Health Alert For Not-Ready-To-Eat Pork And Beef Bacon Products Due to Sodium Nitrite Levels in…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Farmstead Butcher Block LLC
USDA FSIS
Reported Jun 12, 2024
GE HealthCare CRITIKON ONE-CUF blood pressure cuffs, Model numbers: 1. ONE-A1-1B, ONE-CUF, SMALL ADULT, 1 TB BAYONET,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Information Technologies Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Leica HistoCore PEGASUS Tissue Processor, REF 14048858005.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Nussloch GmbH
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Once Upon a Farm Organic Plant-Rich Meal, Curried Carrots & Beans, 3.5 oz, packed in single serving flexible pouches.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Once Upon a Farm Pbc
FDA (openFDA food enforcement)
Reported Jun 12, 2024
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Jun 12, 2024
The Synchro Neuro Guidewires are a steerable guidewire family with a shapeable tip. The outside diameter of the Synchro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Verathon, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2024
Brand Name: Dako CoverStainer, Dako CoverStainer CPO Product Name: CoverStainer, CoverStainer CPO Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Agilent Technologies
FDA (openFDA device enforcement)
Reported Jun 5, 2024
Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG: R16 IPG KIT, REF: M365DB12160, and R32 IPG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jun 5, 2024
BD Pyxis MedStation ES, REF: 323, Medication Cabinet
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2024
FDR Visionary Suite - Intended to generate digital or conventional radiographic images of the skull, spinal column,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FUJIFILM Healthcare Americas Corporation
FDA (openFDA device enforcement)
Reported Jun 5, 2024
Trevo XP ProVue Retriever 4 x 20, Catalog: 90182 Trevo XP ProVue Retriever 3 x 20, Catalog: 90183 Trevo XP ProVue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported May 29, 2024
Brand Name: Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION, ENDOMETRIAL Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Channel Medsystems, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2024
SURGIFOAM" Absorbable Gelatin Powder Kit, Product Code 1979.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2024
Sammy's Milk GOAT MILK TODDLER FORMULA, 25.68 oz (78g) pouch
High riskUsing this product could cause serious injury, illness or death — stop using it now.Graceleigh, Inc. dba Sammy's Milk
1 more product in this recall
FDA (openFDA food 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.