All recall categories

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.

Food

Reported Feb 24, 2016

Pint Umpqua Dairy Cultured Sour Cream, Item no. 03654, net w. 16 oz.; UPC 0 71203 00403 4. Half Pint Umpqua Dairy…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Umpqua Dairy Products Co.

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 17, 2016

Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet France SARL

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2016

Arctic Sun 5000 and Arctic Sun 2000; Intended for monitoring and controlling patient temperatures.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2016

IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Dental Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 10, 2016

Tong Ren Tang Shenjing Shuairuo Wan Herbal Supplement 240 pills UPC Code: 6 904579 129602 Distributed by: Solstice…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Madison One Acme Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 10, 2016

Biosure Driver, Product No: 72201887 For delivery and placement of orthopedic screws. Orthopedic Manual Surgical…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smith & Nephew, Inc., Endoscopy Div.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 10, 2016

This Kid Saves Lives Chocolate Chip UPC #10858497004097 UPC# 858497004090

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

This Bar Saves Lives

FDA (openFDA food enforcement)

Medical devices

Reported Jan 20, 2016

Reprocessed Stryker Color Cuff and Color Cuff II Adult Tourniquet Cuffs Model Numbers: 5921-218-135, 5921-044-135,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Jan 13, 2016

The Fuhrman Pleural/Pneumopericardial Drainage Set The Fuhrman Pleural/Pneumopericardial Drainage Set consists of…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Jan 6, 2016

MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 6, 2016

Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Trumpf Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Vancomycin Screen Agar

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)

Medical devices

Reported Dec 30, 2015

Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Biomerieux

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Boston Scientific, Chariot ST-CCV Guiding Sheath, Sterilized using ethylene oxide: Product Description Material Number…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Reagent Management System (RMS) Dimension EXL with LM Product Usage: The Reagent Management System (RMS) is a module…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

bioMerieux, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

MOSAIQ Oncology Information System. Used to manage workflows for treatment planning and delivery.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2015

Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II, 10 mm, 0 degree, WA50042A ENDOEYE HD II 10 mm,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Nov 25, 2015

Taut Intraducers 10/BX7.5 FR 3.5, Product Code PI-93. To provide an access port into the peritoneal cavity.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex Medical

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2015

Cucumber, sliced 3/8", product is packaged in a 2 lbs. plastic bag and placed in a cardboard box. Product is sold to…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Triple B Corporation

FDA (openFDA food enforcement)

Food

Reported Nov 18, 2015

5/4 Limited Edition Cucumber Carton, Sizes 24SP, 36/36SP, 48. These cucumbers are shipped in a black, green, yellow,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Andrew & Williamson Fresh Produce

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 18, 2015

Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver tips are attached to a surgical drilling unit to carry…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet 3i, LLC

1 more product in this recall

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.