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 Oct 6, 2021

Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or…

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

Deerfield Imaging, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 6, 2021

Elekta Monaco - Product Usage: used to make treatment plans for patients with prescriptions for external beam radiation…

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

Elekta Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 6, 2021

Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack

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

Keurig Dr Pepper

FDA (openFDA food enforcement)

Food

Reported Oct 6, 2021

Little Debbie Mini Nutty Buddy Cookie Bites Sandwich Cookies 2.5oz plastic packaging 72 pouches per case

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

Mckee Foods Corporation

FDA (openFDA food enforcement)

Drugs

Reported Oct 6, 2021

Hydroquinone USP, 4% Skin Bleaching Cream, Rx only, Net Wt 1 oz (28.35g), Manufactured for: Westminster…

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

Monarch PCM, LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Oct 6, 2021

Daytime Severe Cold & Flu Relief 8 Pre-Measured Vials 0.51 FL OZ (15 mL) Each 4.06 FL OZ (120 mL) Total/Nighttime…

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

New Vision Pharmaceuticals LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 29, 2021

Access SARS CoV-2 IgG (1st IS) Assay: Access Immunoassay Systems REAGENT PACK, REF C74339 Access SARS-CoV-2 IgG (1st…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended…

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

In2bones USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only

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

Medtronic Perfusion Systems

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use as an external, non-viable control material to…

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

Microbiologics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 29, 2021

Sodium Sulfacetamide, 10%, Wash, packaged in bottles: a) 6 fl oz (177 mL) NDC 42808-103-06 UPC 3 42808 10306 5; b) 12…

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

Monarch PCM, LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 29, 2021

EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: EPIQ 5 - 795120 EPIQ 5C - 795205…

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

Philips Ultrasound Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System, Catalog Number 09211101190

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

Roche Molecular Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 29, 2021

DAIYA CHEESE VEGAN CHEDDAR STYLE SLICE 8/7.8oz Plastic bag MANUFACDTURED BY: DAIYA FOODS INC., BURNABY, BC CANADA VSA…

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

Sysco Atlanta, LLC

11 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 29, 2021

Kroger Kale Bag 16oz plastic bag 8 packages per case

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

The Kroger Co.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 22, 2021

BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E

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

Carefusion

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

Arjo Disposable Repositioning Sling, Model AHD001

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

Getinge Dominican Republic SA

FDA (openFDA device enforcement)

Food

Reported Sep 22, 2021

Marketside Chocolate Candy Cookie Cake, 24 oz. 12 x 12 black tray with clear lid.

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

Jimmy's Cookies, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 15, 2021

Proteus 235- designed to produce and deliver a proton beam for the treatment of patients with localized tumors and…

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

Ion Beam Applications S.A.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 15, 2021

Pipeline Flex Embolization Device

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

Micro Therapeutics Inc.,

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 15, 2021

MIVI Super 90 Guide Catheters, MIVI Mi-Axus 8F Catheters, REF MIA-9080S (80 cm length); MIA-9090S (90 cm length), and…

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

Mivi Neuroscience Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 10, 2021

FSIS Issues Public Health Alert For Meat Snack Products Containing FDA-Regulated Breadstick Products That Have Been…

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

Fsis

USDA FSIS

Medical devices

Reported Sep 8, 2021

Monaco RTP System, Software Builds 5.40.00, 5.40.01, 5.40.02, and 5.51.10

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

Elekta Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 8, 2021

Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987

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

Hostess Brands, LLC

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.