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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.

4,042 stored notices name Arizona, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Arizona too — those are in the archive.

Medical devices

Reported Apr 18, 2018

Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical device, as part of system to…

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

Reliance Medical Products Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 11, 2018

HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual…

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

C.R. Bard, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 11, 2018

Coconut Smiles - Retail: International Harvest Brand Organic Go Smile! Dried Coconut Raw, in a 9 oz. poly/plastic bag,…

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

International Harvest, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 11, 2018

Oncomine Dx Target Test User Guides and Assay Definition File, Model: A32461; UDI:…

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

Life Technologies Corporation

FDA (openFDA device enforcement)

Food

Reported Apr 11, 2018

King Arthur Flour, 100% Organic, Finely Ground, Coconut Flour, UPC 0 71012 10702 5, Distributed by: The King Arthur…

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

The King Arthur Flour Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 11, 2018

A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts, Item Number: 816209003,UDI: 00887868044670989403

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Ventilator System including Pediatric-Adult…

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

Covidien LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP…

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

DATEX-OHMEDA TEC 7 ANESTHESIA VAPORIZER Is designed for the metered delivery of specific inhalation anesthetic agents…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 04560141940031

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

Konica Minolta Medical Imaging USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device…

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

Mindray DS USA, Inc. dba Mindray North America

FDA (openFDA device enforcement)

Food

Reported Apr 4, 2018

Sour Patch Kids, 1.9 lb bag

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

Mondelez Global LLC

FDA (openFDA food enforcement)

Food

Reported Apr 4, 2018

diet Pepsi Classic Diet Pepsi Taste, 12oz cans, sold as a 12 pk, ambient storage.

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

Pepsico Foods International

FDA (openFDA food enforcement)

Medical devices

Reported Apr 4, 2018

Zimmer M/L Taper Hip Prosthesis, 7711 Series, Femoral Stem 12/14 Neck Taper Plasma Sprayed Press-Fit Cementless Size…

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

Zimmer Biomet, Inc.

19 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI:…

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

Becton Dickinson & Company

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Malecot and the Stenting…

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

Boston Scientific Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; PA023E Probe 7.5/10

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

Esaote S.p.a.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

ClariVein IC infusion catheter, Model Number: 65-018-E4S Product Usage: The ClariVein IC infusion catheter is indicated…

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

Vascular Insights, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 21, 2018

Difco" Agar Noble, 500g bottle Noble Agar is a solidifying agent that is essentially free of impurities. It is used in…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Food

Reported Mar 21, 2018

Kodiak Cakes, Energy Waffles, Blueberry Chia, Net Wt 10.72 Oz (304 g), Kodiak Cakes, Park City, UT. Packaging…

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

Kodiak Cakes, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 21, 2018

OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI:…

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

ZOLL Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI:…

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

Abbott Point Of Care Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 14, 2018

Buttermilk Pancake and Waffle Mix, Item number: 6170B25, packaged in 25 lbs. bulk kraft bag. The label is read in…

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

Bob's Red Mill Natural Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 14, 2018

O-arm¿ O2 interventional fluoroscopic x-ray system; Catalog Number: B1-700-02000 The O-arm O2 Imaging System is a…

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

Medtronic Navigation, Inc.-Littleton

1 more product in this recall

FDA (openFDA device 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.