All recall categories

Recalls distributed in Montana

These notices name Montana 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.

1,662 stored notices name Montana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Montana too — those are in the archive.

Medical devices

Reported Nov 8, 2023

Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets…

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

Quest Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 1, 2023

Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has…

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

Betty Lou's Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 1, 2023

Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack

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

Cardinal Health 200, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 25, 2023

Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777

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

Cardinal Health 200, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 18, 2023

Procedure packs: (1) Presource Pain Tray, Catalog SBAHFPTAS2, Advanced Surgery Center SAR, Sterile. (2) Presource Block…

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

Cardinal Health 200, LLC

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 18, 2023

CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water…

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

RoyalVibe Health Ltd.

FDA (openFDA device enforcement)

Food

Reported Oct 18, 2023

LittleOak Natural Goat Milk Infant Formula (Stage 1); packaged in 800g (1.8lbs) tin cans - six cans per case.

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

The Little Oak Company Ltd.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 11, 2023

JLM Roasted Salted Pecan Halves, 10oz clear plastic container, 12 per wholesale case. Lipari number 368729, UPC…

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

Lipari Foods Operating Company, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 4, 2023

Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 27, 2023

Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 23, 2023

Green Valley Foods Retira Productos Congelados De Pizza De Carne Debido A Un Error De Rotulación Y Alérgenos No…

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

Green Valley Foods

USDA FSIS

Medical devices

Reported Sep 20, 2023

Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product…

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

Abbott Medical

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2023

FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 13, 2023

FSIS Issues Public Health Alert for Kirkland Signature Chicken Tortilla Soup Product Due to Misbranding

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Kettle Cuisine Midco, LLC

USDA FSIS

Medical devices

Reported Sep 13, 2023

ISee Ortho-K Lens

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

PARAGON VISION SCIENCES, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 30, 2023

BioFire Respiratory Panel 2.1 (RP2.1), REF: 423742, For FILMARRAY systems, IVD, Rx Only

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)

Food

Reported Aug 9, 2023

Caesar Pasta Salad is a food service refrigerated product, packaged in 5lb flexible plastic packages, 2/5lb. packages…

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

Eat Good LLC

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 9, 2023

OEC Flexiview 8800 Systems with 9-inch Image Intensifier

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

GE OEC Medical Systems, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…

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

Hamilton Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 26, 2023

Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;…

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

Medtronic Neurosurgery

FDA (openFDA device enforcement)

Food

Reported Jul 19, 2023

Great Value Sliced Strawberries. Item # 107356. Frozen, packaged flexible plastic bags. Net wt. 4 lbs (64oz). UPC on…

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

Oregon Potato Company

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 19, 2023

REF: 218-1604, 1.6mm x 4mm Profile Zero Auto-Drive Screw, Rx Only, Sterile

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

Osteomed, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2023

BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223,…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2023

da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12

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

Intuitive Surgical, 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.