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 Sep 5, 2018
Verigene Enteric Pathogens Nucleic Acid Test (EP) for detecting and identification of pathogenic enteric bacteria,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Sep 5, 2018
Stryker Mako Vizadisc Knee Procedure Tracking Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 5, 2018
QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01520S The Stryker QuickFlap…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Leibinger GmbH & Co. KG
17 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CAREstream Medical LLC
FDA (openFDA device enforcement)
Reported Aug 29, 2018
CIVCO lnfiniti Needle Guide Bracket. used for performing needle-guided (or catheter) procedures with the use of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Civco Medical Instruments Co. Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Driscoll's Only the Finest Berries; Strawberries Fraises; NET WT 16 oz. (1 lb.) Product of the USA Driscoll Strawberry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Driscoll's Strawberry Associates, Inc.
FDA (openFDA food enforcement)
Reported Aug 29, 2018
ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Liebel-Flarsheim Company LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Pasta Spinach with Cavatappi, Reser's Fine Food, item # 71117.14163, 2/4.5 # packages. UPC 0 71117 14163 4. Product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reser's Fine Foods, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 29, 2018
Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Salt & Straw LLC
FDA (openFDA food enforcement)
Reported Aug 29, 2018
The Tri-Flo Subglottic Suction System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vyaire Medical
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Connecting Bolt, Model 14-442093
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2018
Clarity Urocheck 10SG Urinalysis Strips, Model # DTG-10SG Product Usage: Clarity 10SG Urinalysis Reagent Strips (Urine)…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clarity Diagnostics LLC
FDA (openFDA device enforcement)
Reported Aug 22, 2018
20 cm (8") PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer single use,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical de Mexico, S.A. de C.V.
19 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2018
Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Application (PKA) for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Aug 22, 2018
1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2018
Sorin Platinium CRT-D 1711 DF-1, Sterile EO. Implantable Cardiac Defibrillator and Resynchronization Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin CRM SAS
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2018
CDI Blood parameter monitoring system 500 H/SAT, Part No. 145883 Product Usage: The CDI System 500 provides continuous,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Aug 15, 2018
AirLife Resuscitation Device, Adult labeled as the following: a. Adult, with mask, oxygen reservoir bag, Part Number…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vyaire Medical
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.