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 May 24, 2017

Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic…

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

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported May 18, 2017

The Osso Good Co. Recalls Beef and Pork Products Produced Without Benefit of Inspection

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

Yosemite Protein Products, Inc.

USDA FSIS

Medical devices

Reported May 17, 2017

Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box.…

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

Almore International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching

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

Arthrex, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported May 17, 2017

Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin, 60 softgels Rx Only, Manufactured for: Vertical…

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

Vertical Pharmaceuticals, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 10, 2017

MR GHIATAS Beaded Breast Localization Wire, Product Code: 477201, 479201 Product Usage: The GHIATAS Beaded Breast…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2017

The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2017

DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE…

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

Perouse Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2017

Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…

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

Roche Diabetes Care, Inc.

FDA (openFDA device enforcement)

Food

Reported May 10, 2017

Whole Foods Market Cold Pressed Juice, Apple; 16 FL. Oz. (1 pt) 473 mL. Keep refrigerated - Enjoy within 5 days of…

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

Urban Remedy

FDA (openFDA food enforcement)

Medical devices

Reported May 3, 2017

ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14.…

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Food

Reported May 3, 2017

Colby cheese. All affected product private labeled for other companies. Brands: Guggisberg; Dutch Farms; Meijer; Amish…

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

Deutsch Kase Haus, LLC

12 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 3, 2017

Amish Creamery Butter Cheese Sold under the following brand names: Amish Classic 6 lb & 15 ib and Guggisberg 15 ib…

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

Guggisberg Cheese Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 3, 2017

HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a…

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

Heartware

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in…

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

Orthosoft, Inc. dba Zimmer CAS

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood…

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the…

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

Ulrich Medical USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

5.5mm Diameter x 500mm CoCr Straight Rod, Model number X077-0420. The product is packaged in plastic bags with one…

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

Xtant Medical Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Apr 27, 2017

Foster Poultry Farms Recalls Frozen Ready-To-Eat Breaded Chicken Patty Products Due to Possible Foreign Matter…

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

Case Farms, Processing

USDA FSIS

Food

Reported Apr 26, 2017

AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardboard container. UPC 0-23012-00261-9

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

Advanced Fresh Concepts Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 26, 2017

Hemotherm CE, model 400CE, Heater-Cooling Device

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

Cincinnati Sub-Zero Products Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2017

Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product…

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

Covidien Medtronic

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2017

PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture, Manufacturer CP Medical, Portland OR, Sterile, Product Codes…

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

CP Medical 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.