All recall categories

Recalls distributed in Wyoming

These notices name Wyoming 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.

1,195 stored notices name Wyoming, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Wyoming too — those are in the archive.

Medical devices

Reported Aug 10, 2022

EkoSonic Kit 135cm, 12cm TZ The EkoSonic Endovascular Device is packaged as a kit that includes both the USC and IC…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

Merlin PCS 3650 programmer Model 3330 software

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

St. Jude Medical, Cardiac Rhythm Management Division

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 10, 2022

Amaranth Grain Organic, brand Natural Grocers, packaged in plastic bag, net wt. 1 LB (454g) UPC 0 00080 12550 1. Label…

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

Vitamin Cottage Natural Food Markets, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2022

Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si…

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

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2022

Almond Coconut Classic Truffle. Net Wt. 1.4 oz. PLU Code: 788394 11025 2. Ingredients: Milk & dark chocolate, honey,…

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

Queen Bee Gardens, LLC

48 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2022

SX-One MicroKnife

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

Sonex Health LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX,…

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

Cordis US Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

MiniMed 620G Insulin Pump (O.U.S. version)

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

Medtronic MiniMed

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Peak Universal Bond Self-Etch Bottle Kit, Part: 4541; Peak Universal Bond Self-Etch Intro Kit, Part: 4554; Peak SE…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000

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

Zeltiq Aesthetics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…

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

Covidien LLC

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

ABL800 Flex Analyzer Model Numbers 393-800 and 393-801

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

System: Alphenix 4D CT in combination with CAS-930A (C arm Support) Model Number: INFX-8000C/BF, INFX-8000C/BH,…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797

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

Volcano Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 29, 2022

Mini Peanut Butter Cream Pie. Product was available for purchase at the following banner: Haggen. Packaged in clear…

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

Albertsons Companies LLC

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 22, 2022

Cobalt Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Cobalt XT VR: DVPA2D1,…

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

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2022

STORZ KARL STORZ-ENDOSKOPE REF 11272VUE CMOS Video Cysto-Urethroscope REF 11272VUEK CMOS Video Cysto-Urethroscope…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Food

Reported Jun 15, 2022

Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green plastic package.

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

The TJX Companies, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 8, 2022

JIF CREAMY PEANUT BUTTER packaged in 18gram, 500gram, 1 kilogram, 1.1oz (120 count)12oz, 16oz, 28oz, 40oz, 48oz, 4lb…

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

The JM Smucker Company LLC

23 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 1, 2022

Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…

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

Medtronic Neuromodulation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2…

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

Certified Safety Mfg Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…

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

Medtronic Vascular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143

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

Simplivia Healthcare Ltd.

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.