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.
Reported Mar 7, 2018
OTTO BOCK Kenevo knee joints Model 3C60
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Otto Bock Healthcare Product
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
ST AIA-PACK¿ PROG II, Progesterone II Assay, Part Number: 025239
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 28, 2018
IQF Green beans, sold as Not Ready To Eat (NRTE) product for use in foodservice or manufacturing applications. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.National Frozen Foods Corporation--Seattle
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 21, 2018
Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2018
AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO is intended to be used for X-ray computed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Feb 14, 2018
SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible Collar, 10 pack, 45 mm, REF 411802. Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2018
Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported…
High riskUsing this product could cause serious injury, illness or death — stop using it now.J F C International Inc.
FDA (openFDA food enforcement)
Reported Feb 14, 2018
Prickly Ash Bark Powder Herbal Supplement, packaged in food grade stand up plastic pouches or plastic bags depending on…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mountain Rose Inc.
FDA (openFDA food enforcement)
Reported Feb 14, 2018
SunGlow, Unsalted European Style Butter Blend Margarine (16953 SNG), Net Wt 16 oz (1 lb) 454 g. Keep Refrigerated. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventura Foods LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 14, 2018
Wienke's Market Apricot Jam, Net Wt. 8 oz (226g), UPC 14106-00201. Refrigerate after opening. Ingredients: Apricots,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wienke LLC
46 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 14, 2018
DRILL BIT MINI QUICK CONNECT 1.0MM, REF 2312-20-200 & 2312-20-202, NON STERILE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 7, 2018
Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
FDA (openFDA device enforcement)
Reported Jan 31, 2018
MyCareLink Patient Monitors. It is intended for used with a compatible Medtronic patient implanted heart device. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2018
ACCOLADE SR Pacemaker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
23 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2018
Certitude Delivery System and any associated Multipacks Models - 9600CT20A, 9600CT23A, 9600CT26A, 9600CT29A Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jan 17, 2018
SHS Wel-Plan Wheat and Corn Strach Baking Mix , 400 g box,Cardboard carton, 18 cartons per case, but distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutricia North America
FDA (openFDA food enforcement)
Reported Jan 17, 2018
Sundream 12 V tanning bed
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ProSun International, LLC
FDA (openFDA device enforcement)
Reported Jan 3, 2018
Sterile Elastic Esmark Bandage, 3" x 9", individually packaged in a Tyvek plastic form fill seal pouch and placed into…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Dec 27, 2017
Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive investigations of heart and vascular disease when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Dec 13, 2017
TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM), Catalog Number 221261 Trypticase Soy Agar with 5% or 10% Sheep…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2017
Dried Dark Chocolate Covered Cherries, The products are packaged in 25-pound corrugated boxes and 6 oz. and 24 oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shoreline Fruit, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 15, 2017
21st CENTURY SNACK FOODS DARK CHOCOLATE ALMONDS Roasted Almonds Covered in Rich Dark Chocolate Net Wt. 6oz (170g) UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.21st Century Snack Foods
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.