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.
Reported Jul 24, 2019
Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2019
The Tina-quant lgA Gen.2 is an immunoturbidimetric assay. Anti-lgA antibodies react with antigen in the sample to form…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Wilton Chocolate decorator icing stiff consistency 16 oz plastic tub retail unit 6 or 12 retail units per wholesale unit
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Wilton Brands
FDA (openFDA food enforcement)
Reported Jul 17, 2019
Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Jul 17, 2019
Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2019
HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical AG
FDA (openFDA device enforcement)
Reported Jul 17, 2019
ColoCARE, Cat. No. 5650, packaged 250 envelopes/box, For In-Vitro Diagnostic Use. The firm name on the label is Helena…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Helena Laboratories, Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2019
Blue Plate Light Olive Oil Mayonnaise 30oz / 18oz, PET jars and PET squeeze bottles
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Reily Foods Co., Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 17, 2019
Revive Reusable Bladder Support, Model No. 0025 - Product Usage: The Revive bladder support is intended for temporary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rinovum Women's Health
FDA (openFDA device enforcement)
Reported Jul 10, 2019
cobas p 501 post-analytical units, Part Number 05158494001. For diagnostic sample storage and retrieval.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2019
DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2019
Fisher Scientific Isotemp -General Purpose Water Bath: lsotemp 5L GP Bath Model Number: FSGPD05
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thermo Fisher Scientific (Asheville) LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 26, 2019
Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cytocell Ltd.
FDA (openFDA device enforcement)
Reported Jun 26, 2019
CIVCO Solstice(TM) SRS Immobilization System, Part Numbers: a) CHS03, b) CHS04 - Product Usage: The Tilting Head…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med Tec Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2019
IntraClude Intra-Aortic Occlusion Device, REF: ICF100, 10.5 Fr (3.5 mm) X 39.4" (100 cm), Rx Only, Sterile EO The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jun 19, 2019
Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Jun 12, 2019
MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerr/Pentron, dba Kerr Corporation and Pentron Clinical
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F
High riskUsing this product could cause serious injury, illness or death — stop using it now.OriGen Biomedical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula comes inside a package which is labeled in part,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jun 9, 2019
Taylor Farms Illinois, Inc. Recalls Bacon Quiche Products due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms Illinois, Inc.
USDA FSIS
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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.