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 Oct 14, 2020
DABRA RA-308 Excimer Laser, SN: ******* - Product Usage: The device is intended for use in ablating a channel in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ra Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2020
ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2020
Dual Mobility Vivacit-E Bearing, Model Number 110031009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2020
Pacific Xtreme (PTCA Balloon Dilation Catheter)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ev3 Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2020
Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 mm.
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)
Reported Sep 30, 2020
Speed Stitch Needle Cassette
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ArthroCare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2020
BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay, Treponema pallidum:UDI:03610520653012 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2020
NM/CT 850 Model Number: H3907AD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2020
Inquiry Steerable Diagnostic Catheter, REF: IBI-81104 - Product Usage: INDICATIONS FOR USE The Inquiry fixed curve and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Irvine Biomedical Inc., a St. Jude Medical Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Spicy Beef & Vegetables with Rice & Sesame Seeds meal kits containing onions delivered the week of July 27, 2020.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blue Apron Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 23, 2020
The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and communication system software that retrieves,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novarad Corporation
FDA (openFDA device enforcement)
Reported Sep 16, 2020
BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hellofresh US
FDA (openFDA food enforcement)
Reported Sep 16, 2020
MBF-202 Carrageenan
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ingredients Solutions Inc.
FDA (openFDA food enforcement)
Reported Sep 16, 2020
Organic Yellow Popcorn packaged in the following ways: 1) Great Northern Organic Popcorn, Net Wt. 5 Pounds (2.26…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Popcorn
FDA (openFDA food enforcement)
Reported Sep 16, 2020
QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Symbia S-Series and Symbia T-Series - Product Usage: Intended use of the device SPECT: To detect or image the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stimwave Technologies Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2020
CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster (israel), Ltd.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Flexible Intubation Fiberscope, Part: 11301AA1, with Instruction Manual: Z18441US - Product Usage: are intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2020
E.cam or Symbia systems that use foresight detectors - Product Usage: To detect or image the distribution of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Material Number 7002 Unique Tracking Number 1000035843 3/8" Diced Green Chilies (440 lb drum)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sun Valley Foods LLC
FDA (openFDA food enforcement)
Reported Aug 26, 2020
Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
4 more products in this recall
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.