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.
Reported Aug 15, 2018
Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Water Pik, Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
VIDAS LH, Reference Numbers 30406 and 30406-01. Poduct Usage: VIDAS LH is an automated quantitative test for use on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cayenne Medical Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Diamedix Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Instrument trays used to store AltiVate Small Shell Trials (FA S ALTIVATE RSP HUM TRLS SM). Metal container with lid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Aug 8, 2018
MAYFIELD INFINITY XR2 BASE UNIT, Part Number A2079 The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
VNS Therapy Programming System, Rx Only, Model 3000, v1.0.2.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Nicolet¿ Ambulatory EEG
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Zimmer Dermatone AN, Model No. 88710100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Medical Division
FDA (openFDA device enforcement)
Reported Aug 1, 2018
PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies, with caramel flavored chips; NET WT; 2 oz. UPC: 0 31535 59962 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biscomerica, Inc.
FDA (openFDA food enforcement)
Reported Aug 1, 2018
Brivo XR385, model 5215463, Digital Diagnostic Radiographic System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 1, 2018
MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported Aug 1, 2018
ImplantDirect, Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Aug 1, 2018
OMNI Hip System, ApeX-LNK Acetabular Inserts 0 degree, 4+mm offset, Product Codes: H6-14436, H6-13928 & H6-14836…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OMNIlife science Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Superfood Salad Kit - 6.8 lbs. - sold to Kroger owned stores and prepared and purchased at deli department at retail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Papa John's Salads & Produce, Inc.
FDA (openFDA food enforcement)
Reported Aug 1, 2018
BLAST Bandage, sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tactical Medical Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2018
PROLENE SUTURE MONO BLUE - BV1755 Taper Point 3/8C, D10031
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2018
T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Ultrasound & Primary Care Diagnostics, LL
FDA (openFDA device enforcement)
Reported Jul 25, 2018
VOLISTA StandOP Surgical Light, ARD568811961 VLT600DF AIM STP; ARD568821961 VLT600DF AIM STP QL; ARD568811911 VLT600SF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet SAS
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part Number 9735559, Visualase¿ Cooled Laser Applicator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2018
AdvanDx QuickFISH Slides, a component of the QuickFish BC Fixation Kit - BC, REF QFFIXBC1-25, Catalog Number: CS012…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Opgen Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2018
RayStation stand-alone software treatment planning system, RayStation 4.5, RayStation 4.7, RayStation 4.9 (RayPlan 1),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
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.