All recall categories

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.

Medical devices

Reported Oct 3, 2018

DX-D 600 Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imaging system used in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Agfa N.V.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

Bausch + Lomb Stellaris Elite 20 GA Vit Cutter, Model BL5626, 7500 cpm, packaged in sterile pouches, 6/shipper.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bausch & Lomb Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

ESSENTIO Pacemaker

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 3, 2018

FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Confidence Inc./Confidence U.S.A. Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 3, 2018

Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the following product name sold under: Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Medical Systems, LLC

FDA (openFDA device enforcement)

Food

Reported Oct 3, 2018

Shelled eggs in blank cardboard cases at 2.5 dozen a case. Shelled eggs in dozen cartons labeled as "Gravel Ridge Farms…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Gravel Ridge Farms

FDA (openFDA food enforcement)

Medical devices

Reported Oct 3, 2018

Visualase Thermal Therapy System, Software: Visualase Software versions 3.1.1 - 3.2, Product #: 9735542

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Neurosurgery

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

Medtronic DxTerity(TM) TRA 5F, Diagnostic Catheter, REF U5TRAN35

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Medtronic Vascular

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Electronics North America Corporation

26 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

The Shockwave S4 IVL Catheters are intended for lithotripsy-enhanced balloon dilatation of lesions, including calcified…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Shockwave Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2018

400mL, Premium, Urine Meter, 16 FR, Silicone Temperature Sensing Foley Traywith Cath-Secure Plus, Sterile, Item Code…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2018

PR1000 Pivot Rehab Bed AC powered adjustable bed.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Med-Mizer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2018

Endoscopic Cleaning Brush, single use, sold in kits and labeled as the following: a. Item Number DYK1002DCB, BRUSH,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2018

DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Pro-Med Instruments GmbH

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 26, 2018

White Corn Tortilla Chips packaged under the following brand names and sizes: 1. Shearer's White Restaurant Style Bulk,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Shearers Foods, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 26, 2018

Disposable Insulin Syringe 0.3mL in 3 different sizes 29Gx1/2, 30Gx5/16, and 31G x 5/16. (10 syringes are packaged in a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ShinChang Medical Co., Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2018

Gentle Thread PLGA Round Head Interference Screw, 7x20mm, Item Number 905612

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 19, 2018

Beaver Accu-Temp High Temperature Cautery, 2 inch Shaft with Fine Tip, Model Number 8445000 Product Usage: The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beaver Visitec

FDA (openFDA device enforcement)

Food

Reported Sep 19, 2018

Dewey's BAKERY Soft Baked TRIPLE CHOCOLATE BROWNIE COOKIES NET WT. 6 OZ paper bag Dewey's BAKERY WINSTON-SALEM, NC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dewey's Bakery, Inc. dba Salem Baking Company

FDA (openFDA food enforcement)

Medical devices

Reported Sep 19, 2018

da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 19, 2018

Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 280 mm, Item Number: 814309280

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Biomet, Inc.

128 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2018

Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a 10-cc polycarbonate vial (Rx) as follows: Zenlens…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Alden Optical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2018

DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Canon Medical System, USA, Inc.

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.