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.

Medical devices

Reported May 1, 2019

Performance Series Sagittal Blade, Catalog Number 6125-127-100 Product Usage: The Stryker Heavy Duty Sagittal Blades…

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, when used with the…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device intended for use in bony voids or gaps that are…

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

Bioventus, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for…

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

Cordis Corporation

FDA (openFDA device enforcement)

Meat & poultry

Reported Apr 24, 2019

Grant Park Packing Recalls Raw Ground Beef Products Due to Possible E. coli O103 Contamination

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

Grant Park Packing

USDA FSIS

Medical devices

Reported Apr 24, 2019

Salto Talaris, Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Right, Part No. LJU200T

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

Integra LifeSciences Corp.

25 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 24, 2019

NadaMoo! Strawberry Cheesecake Non-Dairy Frozen-Dessert 16 ounce/pint packaged in a carton

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

Little Red Rooster Company

FDA (openFDA food enforcement)

Medical devices

Reported Apr 24, 2019

14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061422

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

Medical Components, Inc. dba MedComp

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed, Model 32/1. Labeled as the following: PROSUN ONYX 32 SLI…

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

ProSun International, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2019

CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are…

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

DePuy Orthopaedics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2019

syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT.…

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)

Medical devices

Reported Apr 10, 2019

The UniCel DxI 600 and 800 Access Immunoassay Systems, that are connected to an automation line. UniCel DxI 600 Catalog…

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

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 10, 2019

Snak Club Honey Bliss Nut Mix: Honey Butter Flavored Almonds, Peanuts, Pumpkin Seeds, Pistachios, Pecans & Honey Sesame…

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

Century Snacks LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 10, 2019

McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178¿TBSO,…

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

Cypress Medical Products LLC

FDA (openFDA device enforcement)

Food

Reported Apr 3, 2019

Modjeskas Bauer's Candies NET WT 8 oz, 12 oz, 16 oz, 32 oz. boxes & 4 oz, 8 oz bags, 400 pc case, 216 pc case

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

Bauer's Candies, Inc.

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 3, 2019

Cardiohelp Emergency Drive, Part No. 70104.8002 Product Usage: The Cardiohelp Emergency Drive is used in emergencies to…

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

Maquet Cardiovascular US Sales, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 3, 2019

Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case)…

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

Medical Action Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 27, 2019

Ne-Mo's Chocolate Cake Square with Cream Cheese Icing, item 104; Net Wt. 3 oz. Case UPC: 2007606401046 4; Display pk 6…

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

Horizon Food Group

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 20, 2019

AVE 2 Birthing Bed

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

Linet Spol. S.r.o.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 20, 2019

Ossur Skull Pin, Sterile Titanium Pin, Part/Description: 516TS/ Skull Pin 2-1/4in TI Sterl 1PK; 516V2S/ Skull Pin 3in…

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

Ossur Americas

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 20, 2019

Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate…

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

Perrigo Company PLC

FDA (openFDA food enforcement)

Food

Reported Mar 13, 2019

DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary…

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

Kingston Pharma LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 13, 2019

Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.

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

Rvo 2.0, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 13, 2019

Big Daddy s Bold Cheese Pizza, item No. 78985. 3-Pack. Contains 9-44.53 oz. Pizzas. Net Wt. 25.04 Lbs. (11.36 kg) For…

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

Schwan's Global Supply Chain, Inc., Specialy Foods Plant

FDA (openFDA food 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.