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.
1,301 stored notices name Alaska, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Alaska too — those are in the archive.
Reported Dec 28, 2016
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
8450-107-530 3.0MM Precision Match Head, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2016
CyberKnife Robotic Radiosurgery System using software version 10.6; Catalog/Part Number: 54000 UDI: M658053301 0…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
FDA (openFDA device enforcement)
Reported Dec 21, 2016
Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm (EMS) The system is intended for use in surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Dec 21, 2016
Performance-LOAD Ambulance Cot Fastener Stretcher, Wheeled
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Brilliance 64 728231 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by…
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 Dec 7, 2016
Monaco RTP System; Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
15 g R.K. Epidural Needle (TW), Catalog #/REF #100-1415 Intended for the epidural placement, directly or through an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epimed International, Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
The Stone Ground Peanut Butter Chocolate Bar, Net wt. 2.5 oz. UPC 8 55966 00107 9.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jjbl LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 9, 2016
Guider Softip XF; GUIDER/40DEG XF/7FR/90CM, Model number: H965100430 . Cardiology: Boston Scientific Guider Softip XF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
14 more products in this recall
FDA (openFDA device 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
Product is refrigerated Boars Head To Go (BTG) Superfood Wrap, sold at deli department. The wraps are made in store…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fred Meyers 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
LipiFlow thermal Pulsation System, consisting of Console and Activator, Model LFD-1100 The LipiFlow Thermal Pulsation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tearscience, Inc.
FDA (openFDA device 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
Sausage, Egg, and Cheese on English Muffin, Fully Cooked, Keep Frozen, Perishable-30/case Manufactured Exclusively for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Progressive Gourmet Inc.
FDA (openFDA food enforcement)
Reported Sep 28, 2016
ULTRA PROTEIN VANILLA¿ 948 grams, packaged in 2500cc White HDPE Canister
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hvl, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 28, 2016
O Organics Vegetable Tray, 18 oz. (1 lb. 2 oz.) 510g plastic tray. Best If Used By: AUG 11 UPC (incorrect, which is on…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mann Packing Company, Inc.
FDA (openFDA food enforcement)
Reported Sep 28, 2016
McKesson Radiology, versions 12.1.1 and 12.2 McKesson Radiology (MR) is a Picture Archiving Communication System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Imaging Group
FDA (openFDA device enforcement)
Reported Sep 28, 2016
RENASYS Sterile Transparent Film and all the RENASYS Dressing kits that contains the RENASYS Sterile Transparent Film…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Sep 22, 2016
RFG Canada Inc. Retira Productos De Pizza De Carne Y Pollo Distribuidos Sin El Beneficio De Inspeccion De Importacin
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
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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.