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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 Mar 13, 2019

Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Phoenix AST-s Indicator, Catalog Number 246009

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

Becton Dickinson & Co.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2019

AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…

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

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2019

Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2019

MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2019

ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a…

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

Abbott Ireland Diagnostics Division

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 13, 2019

Italian Tapenade sandwich is Hoagie sandwich made with pepperoni, salami, capicola, cheese, Tapenade spread and green…

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

Spokane Produce Inc.

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 16, 2019

Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit per Cavity #3 Cavity Deep/20 pieces per case…

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

ICU Medical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G…

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

Medtronic Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2018

enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated for primary implantation for the visual…

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

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2018

VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more of these susceptibility products: Catalog #…

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

bioMerieux, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 5.5 This powder-free sterile light brown colored surgeons gloves are a…

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

Cardinal Health 200, LLC

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 26, 2018

Milk Chocolate Maltballs: NET Wt. 15 lbs. Item number 992 Case UPC 00797817-00992-9 Allergy Information: This product…

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

Marich Confectionery Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 19, 2018

HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx…

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

Philips North America LLC

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2018

16 count Smartfood Delight Variety Pack Sack

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

Frito-Lay, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 5, 2018

Ultra Dark Chocolate Amaretto Rainier Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261…

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

Chukar Cherry Company

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 28, 2018

The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 21, 2018

Rojo's Autentico Black Bean 5 Layer Dip; Layers of Black Beans, Guacamole, Salsa, sour Cream and Cheddar Cheese. NET…

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

Simply Fresh Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 21, 2018

The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option

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

Stryker Medical Division

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 21, 2018

Chef Sensations Fire Roasted 1/2" diced onion/pepper blend Net Wt 20 lbs

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

The Wornick Company

FDA (openFDA food enforcement)

Food

Reported Nov 14, 2018

Pre Proof Danish Net Wt: 13.7lbs (6.2Kg) Contains: Eggs, Milk, Soy and Wheat KEEP FROZEN AT 0 F OR BELOW Bake One, Inc.…

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

Bake One, Inc.

FDA (openFDA food enforcement)

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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.