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 Sep 16, 2020
PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MicroPort Orthopedics Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Whole Foods Market Vegan Vanilla Cake 6 Inch NET WT 2lb 11oz (1219g) Packed for Whole Foods Market PLU 41070 packaged…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
FDA (openFDA food enforcement)
Reported Sep 9, 2020
Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.A. Greiner & Sohne Gesellschaftmbh
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Leiper's Fork Distillery, Alcohol Antiseptic Topical Solution, Ethyl Alcohol 70%, packaged as a) 16 fluid oz./473.18…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leiper's Fork Distillery
FDA (openFDA drug enforcement)
Reported Sep 9, 2020
Symbia S-Series and Symbia T-Series - Product Usage: Intended use of the device SPECT: To detect or image the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stimwave Technologies Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster (israel), Ltd.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Flexible Intubation Fiberscope, Part: 11301AA1, with Instruction Manual: Z18441US - Product Usage: are intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 6.0mm REF NVTKIT-C6-5, Rx Only, Sterile, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neurovision Medical Products Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2020
RayCare, device is stand-alone software - Product Usage: used to support workflows and scheduling, as well as clinical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Sep 2, 2020
E.cam or Symbia systems that use foresight detectors - Product Usage: To detect or image the distribution of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Whole Foods Market Buttermilk Biscuits, 4pk NET WT 1lb 0 oz PLU: 30561 packaged in plastic clam shell
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods Market
FDA (openFDA food enforcement)
Reported Aug 26, 2020
Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2020
HIGH LINER FOODSERVICE***Genuine Maryland-Style Premium Crab Cakes***48-3 oz***KEEP FROZEN***10004302***PRODUCT OF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.High Liner Foods Inc.
FDA (openFDA food enforcement)
Reported Aug 26, 2020
POLARSTEM COLLAR Reamer Guide, Catalog Number: 75102205, UPC Codes: 00885556535493 - Product Usage: Once the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Orthopaedics AG
FDA (openFDA device enforcement)
Reported Aug 26, 2020
Single RIKKI Retractor, Catalog #71934609 - Product Usage: is used during surgery to hold soft tissue away from the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2020
Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smith Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2020
MURRAY'S CHADS SMOKED GOUDA DIP in plastic tubs, all sizes.
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2020
STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is intended to prepare physicians with advanced…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HF Acquisition Co. LLC
FDA (openFDA device enforcement)
Reported Aug 19, 2020
HealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150; Manufactured by HF Acquisition Co. LLC, 11629 49th Place…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HF Acquisition Co., LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Garden Cut Organic Coleslaw w/ Carrots, retail unit packaged in 1lb clam-shell, 4 retail units per wholesale case,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Indianapolis Fruit Company, Inc.
FDA (openFDA food enforcement)
Reported Aug 19, 2020
AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Linet Americas
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
1 more product in this recall
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.