All recall categories

Recalls distributed in Kentucky

These notices name Kentucky 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.

3,340 stored notices name Kentucky, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Kentucky too — those are in the archive.

Drugs

Reported Feb 12, 2014

CHILDREN'S IBUPROFEN, ORAL SUSPENSION, 200 mg/10mL cup BERRY FLAVOR, ALCOHOL FREE, MFG: ACTAVIS, PGK BY SAFECOR…

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

Central Shared Services dba Parallon

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 12, 2014

XiO RTP System. Used to create treatment plans for any cancer patient for whom external beam radiation therapy or…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2014

SuperElastic Regular force NiTi lower or upper Natural arches. 0.16 size 10 or 100 count packages. Highland Metals Inc.…

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

Highland Metals, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2014

3.5mm Locking Cortical Bone Screw, T15 Hexalobe, Self Tapping, 20mm Part No. 00-0903-2620 OrthoPediatrics Pediloc"…

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

OrthoPediatrics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2014

Diagnostic imaging systems (GEMINI LXL Model #882412, TruFlight Select Model #882438, GEMINI TF PET/CT16 Model #882470,…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2014

Walmart Great Value Tex Mex Trail Mix, Net Wt 28 oz (793g), Distributed by Wal Mart Stores, Inc., Bentonville, AR,…

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

Ann's House

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2014

KODAK DirectView DR 7500 Dual Detector System, MODEL DR 7500, Manufactured by Carestream Health, Inc. Made in U.S.A.

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

Carestream Health, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Intended to produce cross-sectional images of the…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

Teflon Tube, sterile T2 Humerus System Stryker Trauma GmbH Prof Kuntscher Str 1-5 24232 Sconkidrchen, Germany…

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

Stryker Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

AnspacSingle use Sterile bone cutting burs.h REF: S-1504TD Twist Drill for 1.5mm x 4mm screw. Rx only Single use…

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

The Anspach Effort, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

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 29, 2014

SIMVIEW NT and SIMVIEW NT with IDI: October 01, 2012 Siemens ceased Simview distribution. Manufactured by: Mecaserto…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 22, 2014

Shredded Swiss Cheese, INGREDIENTS: Milk, Cheese Culture, Enzymes......Aged 60 days. CONTAINS: MILK NET WT. 80 OZ. (5…

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

Biery Cheese Co.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2014

Locking Cortical Screw 3.5mmX38mm REF 8161-35-038

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

Biomet, 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)

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)

Meat & poultry

Reported Jan 17, 2014

Illinois Firm Recalls Sliced Spiral Hams for Possible Listeria Contamination

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

Carl Buddig and Company

USDA FSIS

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

Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only

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

ArthroCare Medical Corporation

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)

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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.