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 May 11, 2022

Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test

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

SML Distribution, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported May 4, 2022

Rebel Pistachio Ice Cream, one pint (473 mL, UPC 8 53149 00821 1, Manufactured by Rebel Creamery LLC, Midway, UT 84049.…

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

Rebel Creamery

FDA (openFDA food enforcement)

Medical devices

Reported May 4, 2022

IMMULITE 2000 Systems HCG [200 Tests, material number 10381206, catalog number L2KCG] and [600 Tests, material number…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

TearCare version 1.0 SmartHubs

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

Sight Sciences, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 27, 2022

Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618,…

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

Respironics California, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 27, 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

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

BenchMark ULTRA and DISCOVERY ULTRA Instruments

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

Ventana Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-3000, Contents: Monitor 1 EA., Accessory Kit 1 EA.

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

Edwards Lifesciences, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762,…

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

Medtronic MiniMed

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material # 10445158, Catalog # K3057 used in the…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 30, 2022

BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372, 7MM], [Item # 110010373,…

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

Biomet, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 30, 2022

Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000

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

Outset Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2022

Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer

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

Bard Peripheral Vascular Inc.

10 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 23, 2022

Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456.…

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

PS Seasoning & Spices, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 16, 2022

CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex

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

Carl Zeiss Meditec, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 16, 2022

Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer

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

Factor

FDA (openFDA food enforcement)

Food

Reported Mar 16, 2022

Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a 12-pack fridge pack carton. UPC…

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

Swire Coca Cola USA

FDA (openFDA food enforcement)

Medical devices

Reported Mar 9, 2022

Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift

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

Acorn Stairlifts, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2022

AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2022

da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 9, 2022

Great Value Restaurant Style White Corn Tortilla Chips, Net St. 13 oz. UPC 78742-11453. Distributed By: Walmart, Inc.…

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

Shearer'S Snacks

FDA (openFDA food enforcement)

Medical devices

Reported Feb 9, 2022

ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 2, 2022

Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individually

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

Brownie Points LLC

FDA (openFDA food 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.