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 Dec 17, 2014

Invacare Perfecto 2 V Oxygen Concentrator The finished device is packaged as a single unit. The service part contains a…

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

Invacare Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 17, 2014

Chicken flavored broth base and seasoning, low sodium sold under the Orrington Farms brand in 5 oz. plastic jars.

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

Kent Precision Foods Group, Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 17, 2014

Margaret Holmes Mixed Greens 14.5 oz, Distributed by McCall Farms, Effingham, SC

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

Mccall Farms Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 17, 2014

Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU.

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

Align Radial Stems, Prosthesis, Elbow, Hemi Replacement of the radial head for degenerative or post-traumatic…

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

Skeletal Dynamics

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT, SIZE 4, LEFT, REF 71425004, QTY 1, Smith & Nephew, knee prosthesis…

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

Smith & Nephew, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…

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

Snug Seat Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / 2.0.3/ (Hi:Art 5.0.1 / 5.0.2 / 5.0.3)

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

TomoTherapy Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Dec 10, 2014

Amerigel Hydrogel Wound Dressing Wound management

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

Amerx Health Care Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 10, 2014

DASANI (R) PURIFIED WATER, 16.9 FL OZ (1.06 PT) 500 mL, BOTTLED BY A MEMBER OF THE COCA-COLA BOTTLERS' ASSOCIATION,…

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

Coca Cola Bottling Company United, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 10, 2014

MAS CardioImmune XL Cardiac Marker Control; Model: CAI-XL1; intended for use in the clinical laboratory as an assayed…

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

Microgenics Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 10, 2014

Queso Seco Centroamericano (Cheese) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Queso…

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

Oasis Brands, Inc.

15 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2014

Gourmet Warehouse, Red Wine Marinade, 16 fl.oz. (473 mL), Ingredient: Soy Sauce, Salt, Black Pepper, Cayenne Pepper,…

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

R and S Gourmet Warehouse

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 10, 2014

Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…

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

Teleflex Medical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2014

ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (sheep) coated…

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

Abbott Ireland Diagnostics Division

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2014

Alfalfa seed: Organic, Alfalfa, NOP Oregon Tilth, Net Wt. 55 LB, International Specialty Supply

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

International Sprout Holding Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2014

LUNA Chest, Model No. LU4006

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

Novadaq Technologies, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2014

Remel TB Potassium Permanganate (.5% Aqueous) 40192, packaged in 250 ml bottles, 5/pkg. A stain for use in qualitative…

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

Remel Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2014

The J700 Floor Mounted Tube Stand (FMTS) is intended to support and position the diagnostic x-ray tube housing assembly…

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

Summit Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2014

Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial…

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

Zimmer, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2014

CyberKnife Robotic Radiosurgery System with the first generation IRIS Variable Aperture Collimator. The CyberKnife is…

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

Accuray Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2014

Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for…

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

Biomerieux

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2014

Edwards Lifesciences Vent Catheters, . Packaged sterile and non-pyrogenic in a sealed, peel-type pouch. Model Numbers:…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2014

AxoTrack I Sterile Procedure Kit 18G, K1001-18XTW, (24/case labeled for US, 5/case labeled for US, 24/case labeled for…

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

Soma Access Systems LLC

FDA (openFDA device enforcement)

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Other states

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.