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 Jul 15, 2026

GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL),…

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

Wallac Oy

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI…

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

Bard Access Systems, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the…

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

Covidien LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1…

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

Hamilton Medical AG

1 more product in this recall

FDA (openFDA device enforcement)

Consumer products

Reported Jul 8, 2026Updated Sep 16, 2026

Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…

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

KAO USA Inc.

FDA (weekly enforcement report)

Food

Reported Jul 8, 2026

MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a…

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

Mars Snacking

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 8, 2026

Radius VSM ECG pre-connected Set, REF: 4842, 4695

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

Masimo Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jul 8, 2026Updated Sep 16, 2026

Apheresis Red Blood Cells, Leukocytes Reduced

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

Medic Inc.

FDA (weekly enforcement report)

Medical devices

Reported Jul 8, 2026

Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…

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

Teleflex LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes…

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

W L Gore & Associates, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jul 8, 2026Updated Sep 16, 2026

Platelets, Pathogen Reduced

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

West TN Regional Blood Center

1 more product in this recall

FDA (weekly enforcement report)

Drugs

Reported Jul 1, 2026Updated Sep 16, 2026

Determine HIV 1/2 Ag/Ab Combo 25T, Model/Catalog No. 7D2648

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

Abbott Diagnostics Scarborough, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Jul 1, 2026

Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL…

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

Acumed LLC

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2026

6/11oz Sunflower Seeds Salted

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

George J Howe Company, Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2026

Da Vinci ASSY, PSS, SP1098, Part Number: 380601

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jul 1, 2026Updated Sep 16, 2026

Apheresis Platelets, Leukocytes Reduced, Irradiated

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

Medic Inc.

1 more product in this recall

FDA (weekly enforcement report)

Medical devices

Reported Jul 1, 2026

INZONE DETACHMENT SYSTEM, REF: M00345100950

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2026

1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.

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

Utz Quality Foods, LLC

5 more products in this recall

FDA (openFDA food enforcement)

Meat & poultry

Reported Jun 25, 2026

FSIS Issues Public Health Alert for Boneless Chicken Breast Product Due to Misbranding and Undeclared Allergens

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

FW Farms LLC.

USDA FSIS

Meat & poultry

Reported Jun 25, 2026

Reser’s Fine Foods, Inc. Recalls Ready-To-Eat Pasta Salad Product Due to Misbranding and Undeclared Allergens

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

Reser's Fine Foods

USDA FSIS

Medical devices

Reported Jun 24, 2026

directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2

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

Accriva Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in,…

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

AMD Medicom Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU

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

Arrow International, LLC

34 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer…

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

Bd Switzerland Sarl

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.