All recall categories

Recalls distributed in Arizona

These notices name Arizona 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.

3,983 stored notices name Arizona, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Arizona too — those are in the archive.

Medical devices

Reported Jun 12, 2019

NxStage PureFlow B Solution, REF RFP-400, M535RFP4000 Product NxStage PureFlow B Solution is indicated for use with…

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

NxStage Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F

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

OriGen Biomedical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Abbott MitraClip XTR Clip Delivery System, UDI: 08717648226366, Part: CDS0601-XTR, Sterile EO, Rx Only

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

Abbott Vascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Horizon Cardiology Hemo

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

Change Healthcare Israel Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2019

Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US

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

Dole Fresh Vegetables

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 5, 2019

First Street Dark Chocolate Nonpareils; 12 oz. stand up re-sealable plastic bags. Ingredients: Sweet Chocolate (sugar,…

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

Heritage Candy Company

FDA (openFDA food enforcement)

Food

Reported Jun 5, 2019

Global Pride Rattan Shoots in Brine: 24 oz. glass jar UPC: 8855273023148 Erawan Enterprise Co. Ltd Bangkok, Thailand.…

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

U.S. Tov, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 29, 2019

EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2019

DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is…

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

KaVo Dental Technologies LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2019

VITROS XT 7600 Integrated System, with V3.4 or 3.4.1 SW Product Code: 6844461 Product Usage: INTENDED USE: For in vitro…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2019

Thio Med w/Dex, Hem, Vit K (5ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general…

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

Remel Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2019

Cobas¿ infinity central lab IT solution Material Number: 07154003001 Calculator/Data Processing Module, For Clinical Use

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

Roche Diagnostics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2019

Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106

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

Zimmer GmbH

75 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported May 23, 2019

Blount Fine Foods Recalls Soup with Chicken Products Due to Possible Foreign Matter Contamination

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

Blount Fine Foods Corp.

USDA FSIS

Medical devices

Reported May 22, 2019

Abbott Alinity ci-series System Control Module software version 2.5.1; LN 3R70-01 with the following hardware: Level…

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent…

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)

Medical devices

Reported May 22, 2019

MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S

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

Compass Health Brands (Corporate Office)

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 22, 2019

Frozen ground tuna, 1 lb package, 20 packages/case

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

Jensen Tuna Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 22, 2019

Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021

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

Moller Vital

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

Artis Zee (material # 10094135, 10094137, 10094141) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of…

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

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2019

Neuro Omega System, incorporating HaGuide software. For neurological and neurosurgical use. To monitor, record and…

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

Alpha Omega Engineering

FDA (openFDA device enforcement)

Food

Reported May 15, 2019

Lee's Tea brand of Pink Chai - Organic Spiced Tulsi Tea Blend Loose Leaf Tea packaged in re-sealable plastic pouches…

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

Lee's Provisions Inc.

FDA (openFDA food enforcement)

Food

Reported May 15, 2019

El Guapo Chile Habanero Habanero Chili Pepper 0.5oz

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

McCormick & Company, Inc. - Flavor Manufacturing Center

1 more product in this recall

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.