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.
Reported Jul 14, 2021
JERSEY COOKIE MONSTER ICE CREAM 3 GALLONS (11.34 LITERS) MFG: GREENWOOD ICE CREAM CO LTD 4829 PEACHTREE ROAD, ATLANTA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greenwood Ice Cream
FDA (openFDA food enforcement)
Reported Jul 14, 2021
Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Heart Valves Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 7, 2021
MaxPlusTM bi fuse extension set with 2 clear needleless connectors - Product Usage: The needleless connector can be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT. Each tray contains 1 of each of the following…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and PET/CT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Lyra SARS-CoV-2 Assay (M120) in vitro diagnostic test reagent
High riskUsing this product could cause serious injury, illness or death — stop using it now.Quidel Corporation
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Tempus Pro - Patient physiological monitor, arrhythmia detector and alarm. Part No. - 00-1004-R, 00-1007-R, 00-1024-R,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Jun 30, 2021
Access SARS CoV-2 lgG II Reagent, REF: C69057, IVD CE UDI: (01)15099590742744
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 30, 2021
inLight Medical LED Pads used with Polychromatic light technology system
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Inlightened Partners LLC
FDA (openFDA device enforcement)
Reported Jun 30, 2021
reSET Mobile App, iOS and Android, provides cognitive behavioral therapy, as part of substance abuse treatment.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pear Therapeutics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 23, 2021
GE Healthcare Innova IGS 3 (GTIN 00840682147378), Innova IGS 5 (GTIN 00840682124621), Innova IGS 6 (GTIN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Medtronic HY10Z48R2, Ctr., Custom Pack HY10Z48R2 Adult ECC 1/4, Custom Perfusion System, Sterile, Rx.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
24 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 23, 2021
BulkFoods.com brand dehydrated chopped celery in 1lb and 5lb plastic bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Natural Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 23, 2021
OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended to provide gross immobilization to the cervical spine. REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04
High riskUsing this product could cause serious injury, illness or death — stop using it now.Avid Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented prosthesis. Part Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Ruffles All Dressed Potato Chips 16 1/8 oz. packaged in flexible plastic bags UPC 28400 56520
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc. Headquarters
FDA (openFDA food enforcement)
Reported Jun 16, 2021
Quickslide GramPro 1 Automated Gram Stanier is a microscope slide stainer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Jun 16, 2021
COVID-19 Self-Test Kit *** INNOVA *** 7T
High riskUsing this product could cause serious injury, illness or death — stop using it now.Innova Medical Group, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
VIA Microcatheter VIA 17 REF VIA-17-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Microvention Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 ,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Mideo's Marinara Glass 32oz jars - 6 jars per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RC Industries Inc.
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.