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 Nov 18, 2015
Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional support during fusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
FDA (openFDA device enforcement)
Reported Oct 28, 2015
XiO Radiation Treatment Planning System. Used to create treatment plans for any cancer patient for whom external beam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2015
Monode, Shortwave Accessory Model #: 02200002 Used in conjunction with the Intelect Shortwave Diathermy 100 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
FDA (openFDA device enforcement)
Reported Oct 7, 2015
Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lifeline Systems, Incorporated
FDA (openFDA device enforcement)
Reported Sep 16, 2015
CDI 500 Blood Parameter Monitoring System. Provides continuous, on-line monitoring of the extracorporeal partial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Sep 9, 2015
Big Train Chai Tea Vanilla Chai, Naturally and Artificially Flavored Drink Mix, No Sugar Added, NET WT 56 oz (3 LB 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerry Foods
FDA (openFDA food enforcement)
Reported Sep 9, 2015
Dark Chocolate with Cranberry, Roasted Nuts & Sea Salt, sold under brand Willit House. Each bar is wrapped in gold foil…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Willit House Chocolate Co.
FDA (openFDA food enforcement)
Reported Sep 2, 2015
ExacTrac 6.0.x Patient Positioning System, Radiation therapy. Intended to be used to place patients at an accurately…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Centricity PACS-IW with Universal Viewer Product Usage: The Centricity PACS-IW with Universal Viewer is a picture…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Kroger Ground Cinnamon UPC 11110 70034 NEW WT. 18.3 oz Plastic container
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 27, 2015
Kapowsin Meats Recalls Pork Product Due To Possible Salmonella Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kapowsin Meats
USDA FSIS
Reported Aug 26, 2015
Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Bronchial Double Lumen Tube Set (Left), Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mason Vitamins, Inc.
FDA (openFDA food enforcement)
Reported Aug 12, 2015
Merge Hemo, 9.10, 9.20.0, 9.20.1,9.20.2, 9.30, 9.40.0, 9.40.1, 9.40.2 with Massimo PHASEIN End Tidal CO2 (EtCO2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Invivo Expression MRI Patient Monitoring System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Aequalis Humeral Nail Targeting Jig, Product Code: 9020060. Orthopedic manual surgical instrument.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2015
American Catheter / Cholangiogram Catheter 9100 Series.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Catheter Corp.
FDA (openFDA device enforcement)
Reported Jul 29, 2015
ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
ADVIA Centaur Tni-Ultra Assay; SMN 10317708 - 100 tests and SMN 10317709 -500 tests Product Usage: For in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2015
0702-001-350Q, Diverter Valve Assembly 0702-001-000, Neptune 2 Rover Ultra (120V) 0702-001-000R, Repair Neptune 2 Rover…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jul 15, 2015
Philips GoSafe Communicator 7000L Personal emergency response system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lifeline Systems, Incorporated
FDA (openFDA device enforcement)
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Other states
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.