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 Feb 5, 2025

Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva", Model 1000 Model/Catalog Number: 1000 Software Version: NA…

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

LivaNova USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2025

Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2025

NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C,D - Height 14 mm, Item Number 00-5994-022-14

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

Zimmer, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

BD PCR Cartridges used with MAX System. Model Number: 437519

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product…

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

Integrity Implants Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product…

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

O&m Halyard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

Brand Name: IMed Products Product Name: Dressing Change Kit with ChloraPrep 3mL & HaloGUARD Model/Catalog Number:…

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

Trinity Sterile, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

McKesson Cardiology Hemo software

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

A L I Technologies Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…

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

Alcon Research LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179

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

Intuitive Surgical, Inc.

38 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810,…

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

Mercury Enterprises, Inc. dba Mercury Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2025

Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack), sterile.

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

Aerin Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 15, 2025

235214 Baker's Source Traditional Cornbread Mix Complete, 5 LB Bags, 30 LB Cases Foodservice Use, Human Consumption &…

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

C.H. Guenther & Son, Inc.

FDA (openFDA food enforcement)

Food

Reported Jan 15, 2025

Grecian Delight Tzatziki sauce, 3.75 lb. tub, UPC 07365000286, SKU SAL028, 4 tubs per case. Sysco Classic Tzatziki…

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

Grecian Delight/Kronos

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 15, 2025

Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25

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

Nipro Renal Soultions USA, Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2025

The FastPack IP Sex Hormone Binding Globulin Immunoassay, Part #25000081, is for the quantitative measurement of SHBG…

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

Qualigen Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2025

Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.

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

Spacelabs Healthcare, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2025

3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self…

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

3M Unitek Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2025

AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100

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

Angiodynamics, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 8, 2025

--- Organic Baby Carrots --- Organic Baby Peeled Carrots 12/12oz Steam-to-Serve; Organic Baby Peel Carrot12/12oz…

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

Grimmway Enterprises, Inc. dba Grimmway Farms

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 8, 2025

Sprout Gyro Family Kit, net wt. 1.750 lb (794 g), food, perishable, plastic tray, 28oz, U UPC 20594800000.

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

Sprouts Farmers Market

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2025

The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming…

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

20/30 INDEFLATOR, REF: 1000184, for use during cardiovascular procedures in conjunction with interventional devices…

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

Abbott Vascular Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

FACSLyric 2L4C Instrument US, Catalog Number 662875, UDI 00382906628756 BD FACSLyric" flow cytometer is intended for in…

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

Becton, Dickinson and Company, BD Bio Sciences

4 more products in this recall

FDA (openFDA device 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.

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.