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 Dec 4, 2019
ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2019
Blue Grass Quality Meats Retira Productos De Cerdo Y Pavo Debido A Un Error De Rotulacin Y Alrgenos No Declarados
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blue Grass Provisions Co. Inc.
USDA FSIS
Reported Nov 27, 2019
EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 20, 2019
Visual-ICE Cryoablation System, FPRCH6000. The cryoablation system is a mobile console system intended for cryoablative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galil Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
ORTHOFIX Catalogue Number: ref 11007, drill bit diameter 4.8 MM LENGTH 280 MM, RX ONLY, Non Sterile, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix Srl
30 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Prismaflex Control Unit, software versions below 7.21
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Kroger Wild Caught Sockeye Salmon Boneless, Frozen, Raw, Skin-on, not ready to eat (NRTE), individually vacuum packed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cold Locker Processing LLC
FDA (openFDA food enforcement)
Reported Nov 13, 2019
Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dollar General Corporation
FDA (openFDA food enforcement)
Reported Nov 13, 2019
SPIFE Alkaline Hemoglobin Kit, Cat. No. 3415, for use in the separation and quantitation of hemoglobins by agarose…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Helena Laboratories, Corp.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Autoject EI, REF AJ1310
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex-Morrisville
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Various products which were contract sterilized.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Anewmed Corporation
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Blue Bell Butter Crunch Ice Cream packaged in a 1/2 Gallon (2 Qts) paperboard cup & lid (4 units per corrugated sleeve,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blue Bell Creameries, LP
FDA (openFDA food enforcement)
Reported Nov 6, 2019
Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the Pediatric Nailing Platform. Product Usage: an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
GANCHI NAIWEITANGPIAN Candy NET WT: 280G(9.8oz) in cardboard package. 24 packages per master case. The following codes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rong Shing Trading Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2019
Glam Day Nougat Candy packaged in 6-ounce (170g) plastic packages containing individually wrapped units identified only…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rong Shing Trading NY Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2019
Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 30, 2019
The ICS CHARTR EP 200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GN Otometrics
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Irrisept Wound Debridement and Cleansing System. 12 units per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IrriMAX Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Premo and Fresh Grab Chicken Salad wheat sandwiches, 5 oz., with UPC code 612510002032.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 30, 2019
Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries 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.