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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.

Medical devices

Reported Feb 20, 2013

Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.

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

Mizuho OSI

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2013

Cloth electrodes with Carbon construction: P/N 201-1231, Cat Nos.: 201-123, 202-454, 203-118, 203-342, 203-454,…

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

NAImco Inc. dba Richmar Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2013

Pamela's Baking and Pancake Mix; Gluten Free, Wheat Free 24 oz package. UPC 93709-30010 Pamela's Products, Ukiah, CA…

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

Pamela's Products, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 13, 2013

Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the…

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

Diagnostic Hybrids Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Exactech NOVATION CROWN CUP, NEUTRAL LINER, Use with Crown Cup Only, GXL UHMWPE, SN 0123456, REF 130-32-53. Exactech…

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

Exactech, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit,…

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

Synthes USA HQ, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle is intended to be recover and detect aerobic…

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No EX500, EX600, and EX700. Used…

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

Cordis Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2013

Growth Factor Complex 200 GFC 200, Dietary Supplement 2 Fl Oz, Manufactured for: Soto Supplements P.O. Box 75774…

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

EonNutra, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2013

Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical…

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

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2013

Extremity Medical, IO FiX System Accessory. Catalog Number 101-00010. This screw measuring device is an accessory to…

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

Extremity Medical LLC

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2013

Food Club Chocolate Chunk Brownie Mix, packaged in 21.5-oz. boxes, UPC# 36800-13486, distributed by TOPCO Associates…

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

Gilster-Mary Lee Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2013

45¿ Angle Driver / Z-H, Greatbatch Medical 10 000 Wahrie Drive, Clarance, NY 14031. Model #: P2661, P2662, T3635,…

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

Greatbatch Medical

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2013

Spice Cake Mix , 25 lb. and 50 lb. kraft bags, labelled a) CMC Quality and Value, Spice Cake Mix, 46702-00985, NET Wt.…

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

Jiffy Food Service, LLC

FDA (openFDA food enforcement)

Food

Reported Feb 6, 2013

Knott's FINE FOODS, CHICKEN SALAD (sandwich), KNOTT's WHOLESALE FOODS, INC. 125 North Blakemore, Paris, TENNESSEE…

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

Knotts Wholesale Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2013

Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.

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

Mindray DS USA, Inc. d.b.a. Mindray North America

FDA (openFDA device enforcement)

Medical devices

Reported Jan 30, 2013

Becton, Dickinson and Company, BBL Crystal Enteric/Nonfermenter ID Kit, Catalog # 24500, cartons of 20 kits, In-vitro…

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

Becton Dickinson & Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 30, 2013

DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Code: 1867-15-870 Spinal Implant Component.

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

DePuy Spine, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 30, 2013

Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Code: BH-2035PE Product Usage: Medisystems Buttonhole…

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

Medisystems a NX Stage Company

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 30, 2013

Roche COBAS INTEGRA 400 and 400 plus Analyzer, an in vitro diagnostic analyzer.

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 23, 2013

Red Apple Slices 2.4 oz, Item #71746, 20 oz, Item # 71729 14 oz, Item # 71735. Item #71729 is sold under the brand name…

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

Fresh Unlimited Inc.

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 23, 2013

Sarns flexible arterial cannula, 6.7 mm (20Fr) OD with 3/8 in. connector, suture ring, 9.5 in (24 cm) long The…

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

Terumo Cardiovascular Systems Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 23, 2013

Woodstock All Natural Tamari Almonds, 7.5 OZ in a gusseted re-sealable poly bag.

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

Woodstock Farms

FDA (openFDA food enforcement)

Medical devices

Reported Jan 16, 2013

FlowGate Balloon Guide Catheter; Manufactured by Concentric Medical, Mountain View, CA.…

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

Concentric Medical 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.