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 Nov 25, 2015
Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2015
Kar's Sweet n' Salty Mix Box of 18, 3.5 oz. flexible film bags. 1 box per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kar Nut Products Company
10 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 25, 2015
c-Budesonide 0.6MG capsules, 60-count bottle, NOT FOR ORAL USE-USE IN NASAL RINSE OR NEBULIZER, SOLUTIONS Rx PHARMACY,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Solutions Rx Pharmacy
FDA (openFDA drug enforcement)
Reported Nov 25, 2015
Taut Intraducers 10/BX7.5 FR 3.5, Product Code PI-93. To provide an access port into the peritoneal cavity.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Nov 19, 2015
Nation Pizza Retira Productos De Mama Cozzi’s Pizza Kitcen Debido A Un Error De Rotulacin Y A Alergnos No…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle USA. Inc.
USDA FSIS
Reported Nov 18, 2015
Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver tips are attached to a surgical drilling unit to carry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional support during fusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
FDA (openFDA device enforcement)
Reported Nov 18, 2015
SSS Reprocessed Zimmer, Synthes, Stryker and Linvatec Drill Bits and Blades Surgical drill bits, blades, burs, chisels,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Myelo-Nate CSF Sampling Kit, Neonatal/Pediatric cerebralspinal fluid sampling sterile tray, including a lumbar puncture…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Utah Medical Products, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WalkMed Infusion, LLC
FDA (openFDA device enforcement)
Reported Nov 11, 2015
ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit ARROW Advantage5 Pressure Injectable PICC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Nov 11, 2015
The Centricity PACS-IW with Universal Viewer is a device that displays medical images (including mammograms) and data…
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 Nov 11, 2015
Robotic hand accessory to InMotion Arm, rehabilitation robot.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Interactive Motion Technologies, Inc.
FDA (openFDA device enforcement)
Reported Nov 11, 2015
Robotic Arm Interactive Orthopedic (RIO) system component PN#205143 (locking pin) and PN# 112220 (connector). Indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Nov 11, 2015
Medtronic Achieve Cables, model 990066. The sterile, single use only Electrical Cable (Model 990066) provides the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
FDA (openFDA device enforcement)
Reported Nov 11, 2015
GEMINI PET/CT System, a diagnostic imaging system for fixed or mobile installations that combines Positron Emission…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Nov 4, 2015
American Pure Whey, Whey Protein Matrix Chocolate flavor, 2 lb. and 5 lb. containers, Manufactured by American Pure…
High riskUsing this product could cause serious injury, illness or death — stop using it now.American Pure Whey
5 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 4, 2015
BD CD3 (SK7) FITC; IVD; Catalog # 349201 and 340542 Hematology: The CD3 antibody reacts with the epsilon chain of the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Nov 4, 2015
CC cartridges for IRMA TRUPOINT Blood Gas Analyzer, PN 039903. The CC Cartridge are single use, disposable, in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LifeHealth, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 4, 2015
Brilliance 16-Slice (Air) Computed Tomography X-ray systems. Intended to produce cross-sectional images of the body.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 4, 2015
2.7 mm Locking Screw SLF-TPNG with T8 Stardrive Recess 12mm. The Synthes modular Mini Fragment LCP System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2015
XiO Radiation Treatment Planning System. Used to create treatment plans for any cancer patient for whom external beam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2015
Taco Seasoning #87469 Net Wt. 9 oz. MFG By Major Products Co., Inc., Little Ferry, NJ 07643 no upc code
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Major Products Company, Inc.
FDA (openFDA food enforcement)
Reported Oct 21, 2015
The Ebb Complete Tamponade System, model #CTS-1000 and Code #OQY. Intended for use in providing temporary control or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clinical Innovations, LLC
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.