Recalls distributed in Alaska
These notices name Alaska 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.
1,282 stored notices name Alaska, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Alaska too — those are in the archive.
Reported Jun 26, 2013
GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2013
XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Atlantic Pro Nutrients, Inc. dba XYMOGEN
FDA (openFDA food enforcement)
Reported Jun 19, 2013
embla Embletta Gold (It functions as a Polysomnography Recorder and Ventilator Effort Recorder). The Embletta Gold is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Embla System LLC
FDA (openFDA device enforcement)
Reported Jun 12, 2013
BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2013
AngioDynamics Micro Introducer Kits under the following labeling: 1) AngioDynamics 4F Standard Micro-Introducer Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 29, 2013
Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported May 8, 2013
STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
FDA (openFDA device enforcement)
Reported May 1, 2013
all One Active Senior Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters
Moderate riskThis product could cause temporary or reversible health problems — stop using it.All One, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 24, 2013
ACIST Medical Systems Inc. The ACIST Angiographic Injection System is intended to be used for the controlled infusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acist Medical Systems
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators; BE 183-SUR and BE 183 SUR-12 Manual Jet…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Industries Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
LHB, Type I First Aid Kit Perishable, Non-Aspirin 4/pg, Aspirin 4/pg and Povidone Iodine, antiseptic towelette. Kit…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lighthouse For The Blind
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2013
NewChapter Probiotic Elderberry, 90 vegetarian capsules bottle. Dietary Supplement UPC: 7-27783-00123-8
High riskUsing this product could cause serious injury, illness or death — stop using it now.New Chapter, Inc.
FDA (openFDA food enforcement)
Reported Apr 17, 2013
G7 HPLC. Used as an aid in the detection and presumptive identification of abnormal hemoglobins in whole blood.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tosoh Bioscience Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Torrent" irrigation tubing. Product Usage: The Torrent irrigation system (tubing and accessories to accommodate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse Berman Angiographic Balloon Catheter. The Arrow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2013
KIMGUARD Container Filters, 7.5in (19cm), Round and 9in. X 9in. (23cm x 23cm), Square. Intended to be used to enclose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
FDA (openFDA device enforcement)
Reported Mar 20, 2013
Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1, R4.2.1, and R4.5.1 Used as part of radiation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 20, 2013
Brilliance 6, 10, 16, 40, 64, Big Bore and the iCT, iCT SP, Ingenuity CT and MX8000 Dual v. EXP are Computed Tomography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 13, 2013
PSX PROXIMATE Skin Staple Extractor, ETHICON ENDO-SURGERY, LLC. For routine skin closure in a wide variety of surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2013
AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization of heat and moisture-stable materials used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Mar 6, 2013
Clover sprouts, product is packaged in a 4 oz or 5 oz. clamshell containers, and 1 lb. bag or 2 lb. tray. Product is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Giant Greens, Inc.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 6, 2013
Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by Philips Medical Systems, Highland Heights, OH…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Animas Corporation
FDA (openFDA device enforcement)
Reported Feb 27, 2013
CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer blood and blood products through a needle or…
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.