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.
Reported Oct 8, 2014
The Symbia T Series consists of the T16, T6, T2, and T. The Symbia T integrates state-of-the-art SPECT and high quality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Hudson RCI¿ Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only, Product Usage: To administer medical…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex Medical
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
CareFusion EnVe and ReVel Ventilators. The EnVe/ ReVel Ventilator is designed for use on patients who require…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 203, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
CareFusion AirLife Heated Infant Breathing Circuit Product Usage: Respiratory breathing circuits are used with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in Centurion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instratek, Incorporated
FDA (openFDA device enforcement)
Reported Oct 1, 2014
The Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN), performed using the sample-to-result Verigene…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nanosphere, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pdg Product Design Group Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Chinese Style Noodles, 10lbs./bx
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phoenix Produce & Noodle Company, LLC.
FDA (openFDA food enforcement)
Reported Oct 1, 2014
EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vidacare Corporation
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Ultraslim. These include all products labeled as UltraSlim, Luxurian, BioSlim Lipo, Cellulize, Slim 'n Trim, UltraRed,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Photonic Systems, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 24, 2014
BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Sep 24, 2014
ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below JResultNet is a stand-alone software package…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Data Innovations, LLC
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Dole Spinach: Thoroughly Washed, Preservative Free Net Wt. 8 oz. bag; Perishable, keep refrigerated. UPC 071430009765…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 24, 2014
Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GF Health Products, Inc./d.b.a.Basic American Metal Products
FDA (openFDA device enforcement)
Reported Sep 24, 2014
AXIOM Luminos dRF system with SW VD10 or on Luminos dRF Max The Axiom Luminos dRF is intended to be used as a universal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Swanson Health Products, Inc.
FDA (openFDA food enforcement)
Reported Sep 17, 2014
PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Sep 17, 2014
Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Force
FDA (openFDA device enforcement)
Reported Sep 17, 2014
Prime Care ¿ Transcend Mattress, Prime Care ¿ Transcend Perimeter Mattress, Prime Care ¿ Transcend Advanced Mattress,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Primus Medical LLC
FDA (openFDA device enforcement)
Reported Sep 17, 2014
RADIANCE v. 2.4X, 2.5X and 2.6X Product Usage: RADIANCE is a data processing application for clinical use intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Sep 17, 2014
Stryker Aria Implant Inserter, REF 48758500, This instrument is part of the Aria product brand. It is used for Implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
1 more product in this recall
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Arizona recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.