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.
4,043 stored notices name Arizona, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported Apr 20, 2016
Diana Automated Compounding System, Diana Onco Plus, Item No. ASN220 The Diana is an automated compounding device for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Brilliance 64:Computed Tomography X-ray Systems, Intended to produce cross-sectional images of the body by computer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Spetzler Claw Tip, Universal - 5450-800-311 Spetzler Open Angle Micro Claw Tip, Universal - 5450-800-313 The Spetzler…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2016
CA500 Epix Universal Clip Applier Product Usage: The Epix disposable laparoscopic clip applier is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) Model Number: MOL2150,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Focus Diagnostics Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute and Chronic Hemodialysis
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2016
GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Inspection Technologies, LP
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Richard-Allan Scientific Paraffin Type 3 For in vitro diagnostic use. For use as an infiltration and embedding medium…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Richard-Allan Scientific Company
FDA (openFDA device enforcement)
Reported Apr 13, 2016
The THERAKOS CELLEX Photopheresis System is a photoimmune therapy. Catalog CLXUSA. Manufacturing lot D342 UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Therakos Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 14mm Sterile. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Manufacturing B.V.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 7, 2016
Pilgrim’s Pride Corp. Retira Productos De Pollo Por Posible Contaminacin De Material Extrao
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pilgrim's Pride Corporation
USDA FSIS
Reported Apr 6, 2016
74" (188cm) approximately 9.0ml, 20 Drop Admin Set w/ Integrated ChemoLock Port sterile IV Administration sets are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
The Spectra-System Dental Implant 2008 system is comprised of dental implant fixtures and prosthetic devices that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Favorites Natural Pistachios, roasted & salted, 4.5 oz (128g) pouch UPC 0 38445 12286 5 Proudly distributed by Circle K…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kanan Enterprises, Inc.
FDA (openFDA food enforcement)
Reported Apr 6, 2016
MAGGI Chicken Flavor Bouillon 6Tab, 12Tab UPC Codes: 028000247959, 028000115678, 028000115678
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle USA
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 6, 2016
Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Thai Fusion Outpost, net weight 5.1 oz. UPC 0 99853 34255 9. Thai Fusion Bulk bag, packaged in a ziploc plastic bag,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Paradise Farm Organics Inc.
FDA (openFDA food enforcement)
Reported Apr 6, 2016
Helios HL3T and HLT Track Mounted Dental Lights Product Usage: The product is intended for use by dental professionals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pelton & Crane / Marus / DCI Equipment / KaVo
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Prosupps Dr. Jekyll INTENSE PUMP PRE WORKOUT, 30 SERVINGS, WATERMELON NATURAL AND ARTIFICIAL FLAVOR DIETARY SUPPLEMENT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ProSupps USA LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 6, 2016
The E.CAM gamma camera system Product Usage: The E.CAM gamma camera system is a SPECT system and measures the…
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 Apr 6, 2016
Synthes Interlocking Bolt, 151 mm (General and Plastics Surgery Devices) Guide, Surgical Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC, Size 3 - Catalog # AR-503-TTTD, Size 4 -Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
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.