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 48,123 notices were distributed nationwide, so they reach Tennessee too — those are in the archive.
Reported Apr 11, 2018
Phadia Prime software, article number 12-4101-00, as used in combination with the Phadia 250 Instrument, article number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia Ab
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Norm-Ject Tuberkulin Syringe, Catalog Number: K-ATS-1000, Global Product Number: G19871 Product Usage: Used to place in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Ventilator System including Pediatric-Adult…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 04560141940031
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Konica Minolta Medical Imaging USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bottles; UPC Code 0 7561654332 6 and Carolina Gold Honey Sauce;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Piggie Park Enterprises Inc.
FDA (openFDA food enforcement)
Reported Apr 4, 2018
The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser is an ophthalmic surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SIE AG, Surgical Instrument Engineering
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Southgate Hot Dog Chili Sauce 15 oz cans UPC 0 71846 95242
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vietti Acquisitions, LLC
FDA (openFDA food enforcement)
Reported Mar 28, 2018
BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Malecot and the Stenting…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
Epi proColon Plasma Quick Kit; Catalog Number: M5-02-001: Consists of 1x Lysis Binding Buffer, 1x Wash B Concentrate,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epigenomics Ag
FDA (openFDA device enforcement)
Reported Mar 28, 2018
GENICON EZEE Retrieval, sterile, Rx only.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genicon, Inc.
FDA (openFDA device enforcement)
Reported Mar 28, 2018
CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
ClariVein IC infusion catheter, Model Number: 65-018-E4S Product Usage: The ClariVein IC infusion catheter is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Insights, LLC
FDA (openFDA device enforcement)
Reported Mar 21, 2018
Difco" Agar Noble, 500g bottle Noble Agar is a solidifying agent that is essentially free of impurities. It is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 21, 2018
Accolade and Restoration hip product; Catalog Number: 6720-0837 and 6721-0737
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 21, 2018
Proteus 235, Uniform and Pencil Beam Scanning The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 21, 2018
OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Medical Corporation
FDA (openFDA device enforcement)
Reported Mar 14, 2018
i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Mar 14, 2018
241-McKesson Premium Skin Staple Remover Kit, Item #100123, McKesson I.V. Start Kit, 100124-McKesson Suture Removal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cypress Medical Products LLC
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Key Lime Pie Handcrafted All-Natural Pop; Net Wt. 3.2 OZ (90g)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King
FDA (openFDA food enforcement)
Reported Mar 14, 2018
O-arm¿ O2 interventional fluoroscopic x-ray system; Catalog Number: B1-700-02000 The O-arm O2 Imaging System is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
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.