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 48,122 notices were distributed nationwide, so they reach Tennessee too — those are in the archive.
Reported Sep 14, 2016
NOMAD Pro Packaged X-Ray System, Part Number 08500009; NOMAD Pro Vet Packaged X-Ray System, Part Number 08500011; NOMAD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aribex Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Arterial Line Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Lysander's Premium Teriyaki Marinade, 1 oz (28 g), polypropylene and clamshell style card, 12 units per case.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Geneva Foods, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 14, 2016
Affinity Four Birthing Bed Model P3700 The primary packaging is pictured below, and utilizes a metal packing brace,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2016
The system provides the ability to transmit patient data files for storage, viewing and analysis at distributed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Merge RadSuite software. Radiological image processing system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 3663202884 packaged in form fill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Dannon Company, Inc.
FDA (openFDA food enforcement)
Reported Sep 7, 2016
Baxter Non-DEHP Micro-Volume Extension Set, Male Luer Lock Adapter, 36 (91 cm), Volume 0.32 mL; an Rx sterile, single…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA device enforcement)
Reported Sep 7, 2016
Geo-Med, TURP/CYSTO PACK PGYBK REF 89-7931.07, Rx Only, STERILE EO, Custom surgical kit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 7, 2016
Centricity Laboratory Core Lab System 4.1 The Centricity Laboratory System is intended to be an information system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare It
FDA (openFDA device enforcement)
Reported Sep 7, 2016
Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Vision Ab
FDA (openFDA device enforcement)
Reported Sep 7, 2016
SPECULAR MICROSCOPE CEM-530; Software version 1.08 and 1.09. Opthalmic: The NIDEK Specular Microscope CEM-530 provides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, Catalog Number 51-7310.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conmed Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site of care.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innokas Medical Oy
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Medtronic, Lead Kit for DBS Stimulation. Model Numbers 3387S-40 (p/n 3387S0007V) & 3389S-40 (p/n 3389S0008V).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. Product Usage: RADIESSE is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
TIGR Matrix Surgical Mesh, Model No. NSTM1015, NSTM1520, NSTM2030
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novus Scientific Ab
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Infinite F50 instrument. The INFINITE F50 instrument is a 96-well absorbance reader for the measurement of light…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Xpert MRSA Catalog GXMRSA-120, Rev. AJ Microbiology: The Cepheid Xpert MRSA assay performed in the GeneXpert Dx System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Al Rasheed Sardine Item #4017 Label not available - NYSDAM sampling.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Greenland Trading Corp.
FDA (openFDA food enforcement)
Reported Aug 24, 2016
Summer Vegetable Salad with Seared Chicken, Garlic Croutons, and Mustard-Chive Vinaigrette
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hellofresh
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 24, 2016
Hospira RECEPTAL CANISTERS: 1L(1000mL), 1.5L(1500mL), 2L(2000mL) Canister, ATS, 2000, with Valve 1) List Numbers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
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.