All recall categories

Recalls distributed in Nevada

These notices name Nevada 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.

2,512 stored notices name Nevada, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Nevada too — those are in the archive.

Medical devices

Reported May 9, 2018

Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3), Product Code EVT45. Accessory Tips for use only with EVICEL…

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

Ethicon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional…

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

Sofradim Production

FDA (openFDA device enforcement)

Food

Reported Apr 25, 2018

Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…

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

Divinity Product Distribution LLC

1 more product in this recall

FDA (openFDA food enforcement)

Drugs

Reported Apr 25, 2018

Ascorbic Acid (Tapioca) 500 mg/mL, 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101,…

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

Partell Specialty Pharmacy

48 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Apr 25, 2018

Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and…

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

Hamilton Medical AG

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 11, 2018

HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual…

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

C.R. Bard, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 11, 2018

Coconut Smiles - Retail: International Harvest Brand Organic Go Smile! Dried Coconut Raw, in a 9 oz. poly/plastic bag,…

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

International Harvest, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 11, 2018

Alpha Air 6 ENT Microscope Microscope examination of the human ear, nose, and throat.

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

Seiler Instr. & Mfg. Co. Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Ventilator System including Pediatric-Adult…

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

Covidien LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP…

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 4, 2018

J.M. Rosen's Cheesecake - New York Traditional; 6 - Unit- 4/46 oz in a case box; Product #56378 UPC 6 93892 99462 7;…

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

J.M.Rosen Cheesecake

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 4, 2018

Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 04560141940031

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

Konica Minolta Medical Imaging USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device…

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

Mindray DS USA, Inc. dba Mindray North America

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI:…

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

Becton Dickinson & Company

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Malecot and the Stenting…

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

Boston Scientific Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in…

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

Medical Components, Inc. dba MedComp

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 21, 2018

NovaKone Daily Wear Soft contact; Catalog Number: AONKS54 Product Usage: The NOVAKONE SPHERICAL lens is indicated for…

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

Alden Optical

10 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Mar 21, 2018

California Jerky Factory, Inc. Recalls Beef Jerky Products Due to Possible Processing Deviation

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

California Jerky Factory, Inc.

USDA FSIS

Medical devices

Reported Mar 21, 2018

OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI:…

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

ZOLL Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI:…

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

Abbott Point Of Care Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 +…

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

Roche Diagnostics Corporation

1 more product in this recall

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.