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 Jul 4, 2018
RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 4, 2018
ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model 10849000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Diagnostic Ultrasound System, Aplio I-series. Labeled as i700, i800, i900 The power supply unit may be damaged and may…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Food Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 4, 2018
Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
CritiCore Automated Urine Output and Temperature Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
VNS Therapy Programmer, Model 3000, v1.0 System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Kellogg's Honey Smacks, 15.3 oz. and 23 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kellogg Company
FDA (openFDA food enforcement)
Reported Jun 27, 2018
P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Birmingham Hip Resurfacing Femoral Head: (a) Size 58 mm, REF 74121158 (b) Size 56 mm, REF 74123156
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls (High 125 ng/ml and Low 75 ng/ml) are used as control…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego Inc. dba Immunalysis Corporation
FDA (openFDA device enforcement)
Reported Jun 20, 2018
XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
37 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Commercial breaders and batters Product B58042 Breader XI- 50 pound bags Product B58915 Breader X1- 40 pound bags…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Newly Weds Foods Inc.
FDA (openFDA food enforcement)
Reported Jun 20, 2018
IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Pious Lion Pure Premium Potent Limited Release Pink Bali, 1 oz plastic bag. 833-AVL-KRTM www.piouslion.com
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pious Lion
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Priano Rosso Pesto Sauce, 6.7oz glass jar
High riskUsing this product could cause serious injury, illness or death — stop using it now.BLM Products U. Vertriebsges
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hobbs Medical, Inc.
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio physiomonitoring system is used to facilitate invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lake Michigan Distilling Co. LLC
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Restoris MCK Onlay Insert Extractor.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Jun 13, 2018
ADVIA Centaur BNP (B-type Natriuretic Peptide), Catalog Numbers: 02816138 (100 tests), 02816634 (500 tests)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products 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.