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 Apr 8, 2015
Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence technology, Brilliance iCT, Brilliance iCT SP,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
LIS27T - Lacrimal Intubation Set RX Only Sterile Used in various ophthalmology procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quest Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm; The 130 Degree Aiming Arm and 125 Degree Aiming Arm are a part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Brand Name: Persona¿ Anterior Referencing Sizer with Locking Boom The Persona Anterior Referencing Sizer is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging is 6 pouches with Tyvek header (9.5 x 13.63 x 3.75")…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ameda, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Coblator II System, 120V. Product Usage: The Coblator II (Model RF8000E) is a bipolar, radiofrequency electrosurgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ArthroCare Medical Corporation
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Mini Naan Eight (8) nann packaged in coated paper printed board and transparent wrap with a net weight of 12.6 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.fgf brands, Inc.
FDA (openFDA food enforcement)
Reported Apr 1, 2015
DUAFIT(R) PIP 0o CA SIZE 2, REF A60 SP002, STERILE R, Rx only. Interphalangeal implant.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.In2Bones, SAS
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2015
The Rheo Knee bionic prosthetic is to be used exclusively for fittings of lower extremity amputations. RHEO KNEE uses…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS, Part Number: 9065 and 9067.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2015
ML 7090 Calibrated LASIK Blade (CLB); CLB CALIBRATED LASIK BLADE 10. ML 7090 Calibrated LASIK Blade (CLB) is to be used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med-logics Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2015
Crea A and B membranes, packaged 4 per box Used in conjunction with the ABL800 FLEX analyzers which are intended for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2015
Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2015
CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2015
TactiSys Quartz Pack, PN-004 400. For percutaneous catheter radiofrequency (RF) ablation of atrial cardiac arrhythmias…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical
FDA (openFDA device enforcement)
Reported Mar 18, 2015
GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Mar 18, 2015
Juno DFR X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Radiology Systems LLC
FDA (openFDA device enforcement)
Reported Mar 18, 2015
Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
SMARTSET GHV Gentamicin Bone Cement. A self-curing, radiopaque, polymethyl methacrylate based cement containing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
Monaco radiation therapy treatment planning system. The Monaco system is used to make treatment plans for patients with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 11, 2015
DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iCAD, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
GROUND CUMIN SEED, 50 LBS NET, ETO STERILE TREATED
High riskUsing this product could cause serious injury, illness or death — stop using it now.Morris J. Golombeck, 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.