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April 14, 2012, 4:00 am by FDA Recalls



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Fitbit Flex Sleep Sensor Tracker

Will health sensors make humans immortal?

Not so fast! We need to get from here to there. Today, health/behavior monitoring and quantification sensors are all the rage. The Fitbit, a wearable sensor, is one of the more popular wearable tech devices for tracking your health. Fitbit tracks your activity (steps), diet, and even your sleep patterns. You can interact with the Fitbit using a series of tapping sequences and the Fitbit syncs all your data with your phone and computer. Then the process is to quantify, analyze, and optimize your wake and sleep life. Doing all this will not help you avoid your ultimate demise, but it could contribute to a longer life and better yet, one where you're in better health along your life's time-line. The concept is that if you are monitoring your activity, food, and sleep, you can make adjustments to improve these areas; thus better health. The Fitbit Flex is only $99! Get started Buy directly from Fitbit

Learn more at Fitbit's Official Website HOT! Fitbit Accessories & New Products Google Fitbit
Matcha Green Tea Super Food Antioxidants

Matcha Green Tea King of Superfoods

Matcha Green Tea is the latest superfood that celebs and regular folk are finding give them supercharged antioxidant purification with a non-jittery sense of focus. Most matcha available to buy is in very small sizes and is not high enough quality. It is important that you buy high quality matcha. We've found bulk high quality 100% natural matcha green tea imported from Japan. Learn more here: Japanese Matcha Green Tea in bulk here on Amazon

High Quality Matcha Find Matcha on Amazon Google Matcha Green Tea

More medical news from FDA Recalls

Cook Medical Issues Global Recall Of Beacon Tip Angiographic Catheter Products
FDA Recalls : August 3, 2015, 5:51 am
On July 2, 2015, Cook Medical initiated a lot-specific voluntary recall of 2,239 lots of Beacon Tip Angiographic Catheters. Globally, 95,167 devices are subject to this recall. The products include specific versions and lot numbers of the Torcon NB® Advantage Beacon® Tip Catheters (Catalog Prefix HNBR5.0), Royal Flush® Plus Beacon® Tip High-Flow Catheters (Catalog Prefix HNR4.0), and Slip-Cath® Beacon® Tip Catheters (Catalog Prefix SCBR5.0).

The Kraft Heinz Company Voluntarily Recalls Select Varieties of Kraft Singles Products Due to Potential Choking Hazard
FDA Recalls : August 1, 2015, 9:25 am
The Kraft Heinz Company is voluntarily recalling select code dates and manufacturing codes of Kraft Singles individually-wrapped slices due to the possibility that a thin strip of the individual packaging film may remain adhered to the slice after the wrapper has been removed. If the film sticks to the slice and is not removed, it could potentially cause a choking hazard.

John B. Sanfilippo & Son, Inc. Voluntarily Recalls Fisher Brand 10 Ounce Chopped Walnuts Because of Possible Health Risk
FDA Recalls : July 31, 2015, 11:18 am
John B. Sanfilippo & Son, Inc. (JBSS) announced today that it is voluntarily recalling Fisher brand chopped walnuts packaged in 10 ounce plastic bags because some of these products may be contaminated with Salmonella.

Baxter Initiates Voluntary Nationwide Recall Of One Lot Of Iv Solution Due To The Potential For Leaking Containers, Particulate Matter And Missing Port Protectors
FDA Recalls : July 31, 2015, 9:21 am
DEERFIELD, Ill., July 30, 2015 - Baxter International Inc. announced today it is voluntarily recalling one lot of intravenous (IV) solution to the hospital/user level due to the potential for leaking containers, particulate matter and missing port protectors. Baxter was made aware of these issues through customer complaints.

Unichem Pharmaceuticals (USA), Inc. Issues a Voluntary Nationwide Recall of Hydrochlorothiazide Tablets Due to the Potential Presence of Foreign Tablets
FDA Recalls : July 31, 2015, 5:42 am
Unichem Pharmaceuticals (USA), Inc. (Unichem) is voluntarily recalling one lot of Hydrochlorothiazide Tablets 25 mg 1000-count bottle to the consumer level. This recall has been initiated as a precautionary measure due to the identification of a Clopidogrel tablet found in a bottle of the product.