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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.

Medical devices

Reported Jan 21, 2026

Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-0002 Software Version:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C-Rad Positioning Ab

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Diagnostica Stago, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 21, 2026

2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

House Of Flavors, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 21, 2026

da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

Medicrea, IB3D Universal Implant Inserter, Rx Only REF: A24000000

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medicrea International

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mobius Imaging, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Thoratec LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2026

BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2026

Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corp. (NeuroSciences)

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2026

Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2026

The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with streptavidin-coated microparticles and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 14, 2026

Town Food Service EQ CO Inc. brand Aluminum Sauce Pans in 1QT, 1.5QT, 2 QT, and 3QT sizes; UPC Codes: 843784003559,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Town Food Service Equip Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 7, 2026

Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 31, 2025

Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

A New Life Herbs, LLC

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 31, 2025

BECKMAN COULTER BICARBONATE REF: OSR6137 OSR6237 OSR6637 OSR6x37 Bicarbonate is a system reagent for the quantitative…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Ireland, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2025

BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2025

Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Draeger, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2025

LifeShield Drug Library Management (DLM); LifeShield Infusion Safety Software Suite v2.2 List Number 17003-02

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2025

da Vinci 5, Surgeon Console Column Motor Connector; ASSY,DV5 CONSOLE,SSC,IS5000; Part Number: 380730-40

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Copan Italia

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

Intelerad InteleShare software, with ProViewer component

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DICOM Grid, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 24, 2025

Linzer Hearts Baked Cut Out Cookies UPC 0 44964 22072 2 72 - 4.0 oz Cut Cookies CBB-220-LZ Net Weight: 18 lbs…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dough-To-Go Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 24, 2025

Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 2…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lexunder Inc.

1 more product in this recall

FDA (openFDA food 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.