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 Jan 29, 2014

VITROS Chemistry Products COCM Reagent

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical Systems, Cleveland,…

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

ABL90 FLEX Analyzer Radiometer Medical ApS, ¿kandevej 21 Br¿nsh¿j, Denmark A portable, automated analyzer that measures…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2014

Centricity PACS System versions 3.X and higher and 4.X and higher Product Usage: The Centricity PACS Workstation is…

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

Ge Healthcare It

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 22, 2014

Hot Smoked Wine Maple Salmon, Item HS-B, vacuum packaged and either frozen or refrigerated, ranging in size between…

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

Josephson's Smokehouse

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2014

Leica BIOSYSTEMS; BOND Polymer Refine Red Detection; Catalog No: DS9390; Leica Biosystems Newcastle Ltd; Balliol…

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

Leica Biosystems Newcastle Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2014

Oxoid Antimicrobial Susceptibility Testing Disc, MEM10, REF: CT0774B, 10 mcg meropenem, Packed in packs containing 5…

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2014

Palacos¿ R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin), 40.8 g Methyl Acrylate Copolymer, 20 ml Methyl…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with the HiLAN¿ and microspeed motor systems to hold…

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

Aesculap, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable Safety Handle with #10 Blade Manufactured for:…

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

Ansell Sandel Medical Industries LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed As GE Healthcare CARESCAPE Patient Data Module)

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

NanoClave Connector, Part No. A1000, Item No. 011-A1000, 061-A1000, A1000, K7083-001, Z3769 The ICU Needleless…

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

ICU Medical, Inc.

49 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

The Vantage Digital Panoramic System delivers high-value features standard on every system: - Five pre-programmed exam…

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

Midmark Corp. dba Progeny Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

Catalys Precision Laser System (United States) - Catalys-U: Catalys Precision Laser System (International) - Catalys I…

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

Optimedica Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe, 1.0ml 29g x 1/2 in Reference: 4429-1…

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

Smiths Medical ASD, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2014

IntelliFill i.v. Pharmacy Compounding Device (PCD). Intended to fill syringes from 0.5mL up to 11.5mL using mixing…

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

Baxter Healthcare Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2014

VERIFY¿ Dual Species Self-Contained Biological Indicator, Distributed by STERIS Corporation, Mentor, OH. Intended for…

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2014

McKesson Radiology 12.0, Picture Archiving Communication System (PACSA).

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

Mckesson Information Solutions LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2014

OrthoPediatrics ACL Reconstruction System is a pediatric and small stature adult ACL reconstruction system containing…

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

OrthoPediatrics Corp.

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2014

Self-Rising White Cornmeal Mix sold under the Aunt Jemima brand and packaged in a paper bag with a net weight…

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

Quaker Foods and Snacks North America

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 1, 2014

Macaroni Reg CAD, Formula MA.50, Macaroni Salad, packaged: -7-Eleven Fresh to Go Macaroni Salad, 12/7-oz carton cases.…

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

Reser's Fine Foods, Inc.

212 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2014

Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging

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

Ziehm Imaging Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2013

DRUK Orange Squash Contains 25% Orange Juice Net Wt. 24 fl oz. Imported by: Balajee Trade Link, LLC Scranton, PA USA…

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

Balajee Trade Link LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2013

outer box: Ref 906768, CurvTek Eye Needle 22 MM X-large Stainless Steel, Single Use Gamma Sterilized, Rx inner…

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

Biomet, Inc.

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.