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 Dec 10, 2014
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…
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 Dec 3, 2014
Karlsburger Foods Taco Seasoning, Item Numbers 43823 (Packaged in 23 oz resealable plastic containers), Item #43807…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Karlsburger Foods, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 3, 2014
Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biomerieux
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2014
10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM - Sterile: intended to treat stable and unstable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Nov 19, 2014
ATTUNE Intuition Distal Femoral Jig; sold non-sterile; product is wrapped in bubble wrap and then sealed inside a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2014
Prescription eyeglass safety lenses. Vision correction
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eyemart Express Ltd.
FDA (openFDA device enforcement)
Reported Nov 12, 2014
CADD-Solis Medication Safety Software, Administrator CD, Version 3.1, REF 21-2194-0301-01. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2014
UNIVERSAL Modular Electric/Battery Handpiece for surgery The electric handpiece is packaged within a foam bag inside of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2014
Laksell Gamma Knife Perfexion
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2014
The GemStar Power Supply is an accessory for the GemStar Infusion Pump. It is a two piece assembled switching power…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2014
ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Accu-Chek Combo System Product Usage: The ACCU-CHEK Combo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Oct 29, 2014
Symbia E is a multi-purpose SPECT system ideal for hospitals and outpatient centers. It is used to detect or image the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2014
Omni Micro-electrode/reference electrode for cobas b221 analyzer. The Roche Diagnostics Omni S Analyzer is a fully…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nemschoff Chairs, Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
The Hulka Clip is a sterile packaged medical device that carries a two year expiration date. It is packaged two clips…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf Medical Instruments Corp.
FDA (openFDA device enforcement)
Reported Oct 8, 2014
The Symbia T Series consists of the T16, T6, T2, and T. The Symbia T integrates state-of-the-art SPECT and high quality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vidacare Corporation
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 24, 2014
BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Swanson Health Products, Inc.
FDA (openFDA food enforcement)
Reported Sep 17, 2014
PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2014
FOCAL Sim Workstation, Radiation Treatment Planning System. Used for patient contouring and viewing of treatment plan…
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)
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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.