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 Dec 18, 2019

Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive, Model Number 701022161. The device is a component of the ROTAFLOW…

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

Maquet Cardiovascular US Sales, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943

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

Medtronic Navigation, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

P28, Titan 3-D Wedge, Evans, Large, 10 mm, sterile, REF P03-EVN-1010-S, Type: Lagrge, Size: 10mm, (01) 00889795018182,…

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

Paragon 28, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2019

Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail bags, 9 bags/case, Packaged by Vitamin…

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

Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2019

Quantam 2000 Electrosurgical Generator, Part number 909075.

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

CooperSurgical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 11, 2019

Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 1PRT(Single Port) Quick Connect…

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

Stryker Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2019

Alinity ci Level Sensor, Bulk Solution

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

Abbott GmbH & Co. KG

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2019

EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxes per case.

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2019

Atellica CH 930 Analyzer

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2019

Ready to eat Pip Pop Movie Theater Popcorn packaged in 24 oz. laminated plastic zip pouch bag, 6 per case, UPC…

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

Water Gardens Confections LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 27, 2019

MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 2 MASKS, Item Code 2040

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

AMD Medicom Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

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)

Medical devices

Reported Nov 27, 2019

Singles carbides by Meisinger, US-No: 245, Sterile R, cylinder round end; US-No 245; Reference: HMUN245-009; Shank:…

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

Hager & Meisinger GmbH

FDA (openFDA device enforcement)

Food

Reported Nov 20, 2019

Carolyn's Cookie Company - Frozen Cookie Doughballs - Bake at Home. Chocolate Chip Net Wt. 22 oz. (623.7g) UPC Code…

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

California New foods

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 20, 2019

Implant Direct, REF654311U, simply InterActive Implant, Surface: SBM, Qty 1, 4.3mmD x 11.5mmL, 3.4mmD Platform, RX…

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

Implant Direct Sybron Manufacturing, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

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)

Food

Reported Nov 13, 2019

Cranberry Chicken Salad, Tuscan Sun brand, is a ready to eat sandwich. Net wt. 9.3 oz (263g). UPC 0 43701 01414 3.…

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

Jumbo Foods, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2019

Grab n Go Opti series VIPR system Model # PRX-9615 - Product Usage: The Grab n Go Opti system is an integrated delivery…

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

Western / Scott Fetzer Company

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

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)

Medical devices

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)

Medical devices

Reported Oct 30, 2019

Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.

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

Candela Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Dole Crushed Pineapple in 100% pineapple juice Manufactured For Dole Packaged Foods, LLC Westlake Village, CA 91361…

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

Dole Packaged Foods, LLC

FDA (openFDA food enforcement)

Medical devices

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)

Medical devices

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)

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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.