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 Oct 23, 2024

Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR BLUE Model/Catalog Number: 4329BL Product Description:…

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

Nova Ortho-Med Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2024

FastPack TSH Calibrator Kit, REF: 25000024, For use in conjunction with the FastPack IP TSH Immunoassay and FastPack IP…

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

Qualigen Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2024

Aligned Medical Tonsil Tray REF AMS9300A that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a…

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

Windstone Medical Packaging, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2024

DAILIES TOTAL1, DAILIES TOTAL1 for Astigmatism, DAILIES TOTAL1 Multifocal, TOTAL30 Sphere,

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

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2024

MiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714, MMT-1715, MMT-1754, MMT-1755; MiniMed 700G Insulin Pump, REF:…

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

Medtronic MiniMed, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2024

Tablo Console, REF: PN-0003000, PN-0006000, part of the Tablo Hemodialysis System. The Tablo Hemodialysis System is…

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

Outset Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 2, 2024

Montreal Fudge brand Chocolate Fudge with Nuts; 5.6oz

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

Authentik Fudge

FDA (openFDA food enforcement)

Medical devices

Reported Oct 2, 2024

Karl Storz - Endoskope , REF: 27092AMA, Hopkins Telescope 6, Rx only, CE 0123

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

Karl Storz Endoscopy

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2024

ACUSON Juniper 1.0, 1.5, 2.0, 2.5 Diagnostic Ultrasound Systems, REF: 11335791, with software. ACUSON Juniper Select…

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

Siemens Medical Solutions USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2024

FILMARRAY 2.0 INSTRUMENT, REF: FLM2-ASY-0001, FLM2-ASY-0001-W

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

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2024

Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States:…

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

W L Gore & Associates, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2024

FreeStyle Libre 3 Sensors, REF: 72081-01, component of the FreeStyle Libre 3 Continuous Glucose Monitoring System

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

Abbott Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2024

McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only

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

Covidien

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2024

Disposable 5 Lead Cable and Lead Wire System, 50 inches, REF: LW-309DS50/5A

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

Cepheid, Sample Collection Device, Part: 900-0370

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

Cepheid

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Rapid…

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

Merit Medical Systems, Inc.

22 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2024

BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI)…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2024

BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, for FILMARRAY Systems, when used in…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2024

Corey B's Oh Baby BBQ Sauce packaged in 12.6oz glass flask - 12 bottles per case

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

Hoff & Pepper, Co. LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 7, 2024

Arctic Sun Temperature Management Systems, Name/REF: Arctic Sun STAT, NA/6000-00-00; Arctic Sun STAT Loaner,…

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

Medivance Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2024

Diamond Shruumz Infused Cones Cookies and Cream UPC 810133320025

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

Prophet Premium Blends, LLC

21 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 31, 2024

Abbott Infinity 5, Implantable Pulse Generator, REF: 6660, SterileEO, Rx Only

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

Abbott Medical

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2024

Beckman Coulter, REF: OSR61173, IGM 4x14 mL R1, 4x11 mL R2

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

Beckman Coulter Inc.

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.