All recall categories

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 Sep 24, 2025

Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number: 92328632-09

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2025

Exactech Equinoxe, Reverse Shoulder Humeral Liners, REF: 320-38-00,145-DEG PE 38MM HUM LINER +0/ 320-38-03,145-DEG PE…

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

Exactech, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 24, 2025

FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADRANGULARIS SUPPORTS TENDONS & MUSSCLES PROMOTES HEALTH…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Hi-Tech Pharmaceuticals Inc.

15 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 24, 2025

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+…

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

Max Mobility LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2025

Pinnacle Radiation Therapy Planning System: Multimodality Simulation Workspace 18.0.5 Model 870258 UDI code:…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 17, 2025

Peanut rounds 2.25 oz and 3 oz

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

Anderson Candy Company, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 17, 2025

Brand Name: Fortress Introducer Sheath System Product Name: Fortress Introducer Sheath System Model/Catalog Number:…

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

Contract Medical International GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 mm x 100 um, SterileEO, RX…

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

Corneat Vision, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD Model/Catalog Number: 804-06-311…

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

Encore Medical, LP

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 17, 2025

Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with…

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

M.O.M Enterprises, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 17, 2025

NOxBOXi Nitric Oxide Delivery System

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

Noxbox Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

QuickVue: Dipstick Strep A Test: 50T, REF: 20108; 25T, REF: 20125; 50T, SCN, REF: 20108SC

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System

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

Seaspine Orthopedics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

Artis Pheno. Image-Intensified Flouroscopic X-Ray System.

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2025

Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect…

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2025

Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿…

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

Integra LifeSciences Corp. (NeuroSciences)

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2025

Lemon Meringue Pie, 8" round. Net Wt. 27 OZ; Refrigerate after opening Item Code 31811; UPC: 8 85523 31811 1;Jessie's…

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

Jessie Lord Bakery, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2025

Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2025

Panko Style Breaded Butterfly Shrimp (16/20 CT per pound) in bulk packaging, corrugated master cartons. Master carton…

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

Tampa Maid Foods, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 10, 2025

Salad Kit labeled as follows: Taylor FARMS Honey Balsamic SALAD KIT, NET WT. 8.3 OZ (235g), INGREDIENTS: HONEY BALSAMIC…

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

Taylor Farms Retail, Inc.

FDA (openFDA food enforcement)

Food

Reported Sep 3, 2025

Baker's Authority Three Seed Mix; 5lb bag; stored dry at room temperature; packaged in silver bag

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

Bakers Authority LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2025

BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2025

Chocolate Chip Cookie Dough ice cream cartons with a Moo-llennium Crunch lid. Packaging contains Moo-llennium crunch.…

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

Blue Bell Creameries, LP

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2025

BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis"…

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

CareFusion 303, Inc.

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.