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.
4,045 stored notices name Arizona, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,853 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported Dec 12, 2012
OmniGuide BP-ROBOTIC ( BeamPath Robotic), Single Use Cat. # BP-ROBOTIC The OmniGuide Fiber is indicated for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OmniGuide, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Ground limestone also known as calcium carbonate. Omya's food grade ground limestone products. All bulk with no product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Omya Inc.
FDA (openFDA food enforcement)
Reported Dec 12, 2012
Cobas 8000 Modular Analyzer Series, Model/Catalog/Part Number: 05641489001. The Cobas 8000 is a fully automated system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Echo Bi-Metric Press-Fit Stems/Echo Bi-Metric 11mm x 135mm Collarless Porous Stem (Orthopedic Implant) Indications: 1)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Dec 5, 2012
IO FiX X-Post Reamer, Extremity Medical, www.extremitymedical.com; Customer Service: 888.499.0079 The X-Post Reamer is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Dec 5, 2012
The brand name is MRidium Series 1000 MR Infusion Sets, Type 1058 MR IV Extension Set, Lot Code LBG001. The generic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Iradimed Corporation
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Kroger Deluxe French Vanilla Magnifique Ice Cream, 48 FL OZ laminated carton. INGREDIENTS: MILK, CREAM,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Co.
FDA (openFDA food enforcement)
Reported Dec 5, 2012
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
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 Dec 5, 2012
Chicken of the Sea Solid White Tuna in Water, 7 oz., 48 cans per case (case: 6 sets of multi-unit packs of 8 cans…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tri-Union Seafoods, L.L.C dba Chicken of the Sea.
FDA (openFDA food enforcement)
Reported Dec 5, 2012
NexGen CompleteKnee Solution Stemmed Nonaugmentable Tibial component The NexGen¿¿ system is a semiconstrained,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
bioMerieux BacT/ALERT Control Module, catalog number 210147, Clinical instrument The product is most commonly used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
31 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
IO Fix IntraOsseous Fixation System; Extremity Medical. www.extremitymedical.com; Customer Service: 888.499.0079. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Nov 28, 2012
The RIO (TGS 2.), Model # MAKO TGS 2.0 (Part No. 204000). The RIO is intended to assist the surgeon in providing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent Cartridge (K4071) The THEO method is an in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Styker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical Hemostat. Sterile, single use device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Orthobiologics, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Salted in-shell Peanuts under the following. Salted in Shell PeanutsGless Ranch Label, Item Number 450-175, Pack Size…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Torn & Glasser Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 28, 2012
Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal scalp circular (spiral) electrode and applicator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Signs Devices, a GE Healthcare Company
FDA (openFDA device enforcement)
Reported Nov 21, 2012
Albertsons Peanut Butter Cup Ice Cream, 1.5 QTS (1.42 L)(vanilla ice cream with peanut butter cup pieces, fudge and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dean Foods Company
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 21, 2012
Aunt Marie's Bakery Gourmet Cookie Dough, Chocolate Chunk, packaged in 3-lb. plastic tubs. Distributed by Racine Danish…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RDK Corp.
FDA (openFDA food enforcement)
Reported Nov 14, 2012
Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 (List Number 06F12-09; Lot Number 071039) Cliniqa Liquid…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clinical Diagnostic Solutions
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Starbucks Protein Bistro Box, Net Wt 6.8 OZ (193g), Contains Cage-free egg, white Cheddar Cheese, multigrain muesli…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Flying Food Group, Inc.
FDA (openFDA food 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.