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 Nov 2, 2016
Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
FDA (openFDA device enforcement)
Reported Nov 2, 2016
DM Light Slices Yellow Cling Peaches -15 oz (425g) 300 x 407
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Research Center - Walnut Creek
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Awareness Corporation
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Endoscopic Articulating Linear Cutter, ATB35. Standard 35 MM. The ENDOPATH ETS-Flex Endoscopic Articulating Linear…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
HeartWare Ventricular Assist System Controller Product Usage: For use as a bridge-to-cardiac transplantation in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Oct 26, 2016
OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Oct 26, 2016
FI Dry Blueberry / Strawberry Blend, Product Code 21585. 40 lb corrugated case with polyliner. Manufactured by:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.QualiTech, Inc.
17 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Calix P PEEK Lumbar System, PLIF Rasp
Moderate riskThis product could cause temporary or reversible health problems — stop using it.X Spine Systems Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2016
The Introes Pocket Bougie is an endotracheal tube introducer. The device is an endotracheal tube introducer and it is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brathwaites Oliver Medical
FDA (openFDA device enforcement)
Reported Oct 19, 2016
OEC Brivo 715 Prime, OEC Brivo 785 Essential, OEC Brivo 865 Advance Product Usage: The OEC Brivo Mobile C-Arm X-Ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
HeartWare Ventricular Assist System (HVAD), US product: Model No.: 1103; and International Product: Model No.: 1104XX.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare, Inc.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
Radiation Therapy Treatment Planning System, Model 5.0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Oct 19, 2016
BioSentry Tract Sealant System, Product Code: 768022019S; Indicated to provide accuracy in marking a biopsy location…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Surgical Specialties Mexico S DE RL DE CV
FDA (openFDA device enforcement)
Reported Oct 19, 2016
Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 12, 2016
BLUE IMPERVIOUS GOWN WITH THUMBHOOKS, X-LARGE. Non-Sterile, Single Use Only, Plastic Non-Surgical Isolation Gown…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health
FDA (openFDA device enforcement)
Reported Oct 12, 2016
Coca-Cola, 16 fl. oz. can/12 pack, UPC 049000054318; Coca-Cola, 12 oz. can/12 pack, UPC 049000028904; Coca-Cola Zero,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coca-Cola Company (The)
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 12, 2016
Zenostar MT Color Impulse blue, Art. no. 681165 Product Usage: For coloring dental porcelain
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ivoclar Vivadent, Inc.
20 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 12, 2016
Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography X-ray systems intended to product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 12, 2016
Diamond of California¿ Chopped Macadamia Nuts 4oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.Snyder's-Lance Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 12, 2016
Sunflower Kernels packaged in the following brands and sizes: UPC 041498206680, Southern Grove Roasted and Salted…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Treehouse Foods
54 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 5, 2016
The EKOS cart has the catalog number 700-60101. The EKOS cart is a custom infusion stand/cart used to hold and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.EKOS Corporation
FDA (openFDA device enforcement)
Reported Oct 5, 2016
DRI Salicylate Serum Tox Assay, Catalog number 0977. Toxicology: The DRI Salicylate Serum Tox Assay is intended for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Oct 5, 2016
BruxZir Shaded, Model No. 70-1167-NOW0001, 70-1167-NOW0002, 70-1167-NOW0003, 70-1167-NOW0005, 70-1167-NOW0006 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prismatik Dentalcraft, 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.