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 Oct 9, 2013
Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The intended use is in vitro testing of samples of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Fancy Mixed Nuts (25lbs), Mixed Nuts (25lbs), and Super King Fancy Mixed Nuts (25lbs)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Nut Company
FDA (openFDA food enforcement)
Reported Oct 2, 2013
BD Epilor Syringe BD Franklin Lakes, NJ 07417 BD EDC Laagstraat 57, B-9140 Temse-Belgium The Epilor syringe is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Oct 2, 2013
SmartSite Low Sorbing Infusion Set, Model#72313E The SmartSite Low Sorbing Infusion Sets are used to administer fluid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2013
GE 1.5T Signa HDxt, 3.0T Signa HDxt, Signa Vibrant, HD23 Software and the following model numbers: 2395001, 2395001-2,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Oct 2, 2013
First Street Blueberry Muffins (S 45395), 14 oz., 9 trays/case, UPC 0 4151210833 4
High riskUsing this product could cause serious injury, illness or death — stop using it now.KDK Management, Inc., dba Bubbles Baking Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 2, 2013
Almond Biscotti, 1 oz. and 0.5 oz. wrapped in plastic, with "Enjoy By dates prior to 091614, manufactured by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Semifreddi's Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 2, 2013
Smith Medical, Deltec, REF 21-2386-24, 11 Fr Introducer Set with Peel-Away Sheath, Sterile EO, Rx Only PORT-A-CATH¿ and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Stryker Vision Mounting Arm, for use with other Stryker Endoscopy medical device products for human patients. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Endoscopy
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Terumo Pall AL6X Arterial Blood Line Filter, labeled in part Terumo Cardiovascular Systems Corporation, packaged as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Dannon ACTIVIA¿ LIGHT Nonfat Yogurt Strawberry-Banana & Peach Flavor, 12 PACK of 4oz cups, Form fill seal 4oz cup
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Dannon Company, Inc.
FDA (openFDA food enforcement)
Reported Sep 25, 2013
3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6. Intended for use in constructing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Sep 25, 2013
DiaScreen Liquid Urine Controls: Positive and Negative Assayed Liquid Quality Controls for use with Dipsticks in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Assuramed
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Olde Cape Cod Chipotle Ranch dressing, 16 oz. Item Number: 90997-11630
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cains Foods LP
FDA (openFDA food enforcement)
Reported Sep 25, 2013
Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Pills bury Cinnamon Rolls with Icing, CINNA BON, USPC 1800000501, 1800052230, 12.4 oz and 2-pack USPC 1800045675,2-…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
FDA (openFDA food enforcement)
Reported Sep 25, 2013
ACL TOP (Base); PN 0000280000 Bench top, fully automated, random access analyzer designed specifically for in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory Co.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Brilliance CT 6, M/N 728256; Brilliance CT 16 M/N 728246; Brilliance CT 40, M/N 728235 & Brilliance CT 64 M/N 728231,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Responder 5 is a nurse call communication system that connects patients with staff in a hospital. The nurse call system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rauland-Borg Corp.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Sonogage EyeScan, A-Scan Biometer, Product Usage: A-Scan Biometer diagnostic device for measurement of axial eye length.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sonogage Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
AEQUALIS Reversed II or AEQUALIS Reversed Fracture Impactor. These products are contained within the Aequalis reversed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Juno DRF System. Mobile X-ray system These are general, multi-function x-ray systems capable of routine radiographs and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Radiology Systems LLC
FDA (openFDA device enforcement)
Reported Sep 18, 2013
OPERON D850 Surgical Table Product Usage: Surgical Table
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Berchtold Corp.
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.