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 Sep 10, 2025

Medshape Universal Joints, REF: DNE-9000-UJ

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

Medshape, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis"…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

IPC Powerease System REF 2300000 UDI-DI: 00613994448705 00643169406834. The IPC POWEREASE System is indicated for…

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

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2025

Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz twin pack UPC 8 88109 01002 7; 10-1.28 oz carton (12.7…

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

The J.M. Smucker Company

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2025

Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The…

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

THOR Photomedicine Ltd.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2025

Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep…

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 27, 2025

Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. Side panel reads:…

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

Khee Trading, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 20, 2025

FG60005 Blueberry Basil Lemonade

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

And Go Concepts dba Salad and Go

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 20, 2025

Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray…

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

Carefree Surgical Specialties

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2025

Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 20, 2025

Clover Valley Instant Coffee, NET WT 8 OZ (227 g), packaged in a glass jar, packed 6 jars per case, UPC: 876941004069,…

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

Dollar General Corporation

FDA (openFDA food enforcement)

Food

Reported Aug 20, 2025

Sukhi's CLASSIC CURRY PASTE, Net Wt. 2.5 LBS, ITEM # 11-101, UPC: 7-67226-01001-4, SUKHI'S GOURMET INDIAN FOODS…

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

Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian Foods

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 13, 2025

Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.

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

B Braun Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2025

BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 13, 2025

Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.35OZ (10g) STRAWBERRY POUCHES 5-0.42OZ (12g) BANANA POUCHES…

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

Doehler North America, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 6, 2025

SafeStar 90 Plus Filter. Bidirectionally breathing system filter.

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

Draeger, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site (Qty 25). Product Code: SET-0013-25.

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

Fresenius Kabi USA, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop…

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

Implant Direct Sybron Manufacturing LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700,…

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

Volcano Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and…

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 Jul 30, 2025

Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N,…

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

Covidien

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.