Tuesday, July 12, 2011

Banned Chemicals in Fish!

Banned chemicals found in tons of imported fish found for sale in the U.S.
Fish from overseas that are contaminated with chemicals not allowed in the U.S. food supply are showing up for sale in this country, including in Tennessee. Three American fish importers pleaded guilty earlier this year in Mobile, Ala., to federal felony charges of mislabeling fish and seafood. Their illegal haul included more than 120,000 pounds of imported fish, brought in to Mobile and Seattle, that tested positive for the suspected human carcinogen malachite green, an antifungal agent, and for an antibiotic that U.S. authorities also prohibit for use on fish that people consume.

Over the past 12 months, officials in Tennessee, one of the few states doing testing, found evidence of a prohibited substance. Alabama, Georgia, Arkansas and Florida also turned up the same in recent years while screening imported fish. How much tainted fish might end up on plates in restaurants or homes is unknown, but one Alabama official says it’s coming into the country despite a U.S. Food and Drug Administration effort to block such shipments. “I can tell you right off the bat that 40 percent of the imported fish we test is positive for banned drugs that are not safe for human health,” said Brett Hall, deputy commissioner for the Alabama Department of Agriculture and Industries.
The U.S. Government Accountability Office issued a report in April saying improved FDA oversight is needed of imported seafood, with recommendations to better leverage limited funding.


Antibiotics Found
Over the past year, Georgia and Arkansas found evidence of fluoroquinolones, a banned family of antibiotics, in imported fish. Arkansas detected crystal violet, a carcinogen. In February, fluoroquinolones residue was discovered in imported fish in Tennessee. Out of 17 imported basa — a mild-tasting Asian catfish — and other catfish samples analyzed, one was positive for the illegal antibiotics over the past year, according to the Tennessee Department of Agriculture. That was using the FDA’s tolerance standard of 5 parts per million. No imported shrimp samples have shown a problem. “We began testing imported fish about five years ago due to growing consumer concerns,” said Casey Mahoney, a department spokeswoman.

After the one positive sample among 78 lots since testing began in July 2006, the distributor was notified and a recall was initiated. Delivery drivers were told to collect any basa fish remaining and deliver them back to the distributor’s warehouse, where the product was destroyed. The product was originally distributed to food service establishments. Tennessee does quarterly sampling and testing at wholesale and retail establishments. Alabama started such testing earlier and has now dropped it because of funding shortages. From 2002 to 2009, Alabama records show, 44 percent of basa fish it sampled from Asia were positive for fluoroquinolones, prompting the state to issue nine “suspensions from sale or movement orders” to take the fish off the market.
The United States today imports almost 85 percent of its seafood, and about half of it is from aquaculture, which frequently uses antibiotics to control disease. Most of the seafood comes from China, Thailand, Canada, Indonesia, Vietnam and Ecuador.



Article from:
www.fairwarning.org and Anne Paine The Tennessean

Monday, July 11, 2011

3 Party Food Safety Audits on-board U.S. Maritime Vessels

Are third party food safety and sanitation audits (inspections) really necessary on-board U.S. Maritime commercial vessels? Having been on-board a number of vessels the past three years, I have found these audits (inspections) critical in the process of creating a food safety system to control food bourne risks. Who is the regulatory authority that governs the inspections of maritime vessels? On land we have the local Health Department that is the regulatory authority that does carry outs the inspection of food operations. But, most maritime vesssels rely on internal procedures to control food bourne risk factors.


Our firm has developed a system for food safety and sanitation inspections on-board maritime vessels in the U.S. We also developed Active Managerial Controls and Standard Operating Procedures to control food bourne risks. If you are a U.S. maritime company and want more information on our services, contact us at: chef@americanchefconsulting.com

Thursday, July 7, 2011

Possible Listeria Contamination

Hawaii Firm Recalls Convenience Meals for Possible Listeria Contamination

Recall Release CLASS I RECALL
FSIS-RC-047-2011 HEALTH RISK: HIGH


WASHINGTON, July 6, 2011- Warabeya U.S.A., Inc., a Honolulu, Hawaii establishment, is recalling approximately 1,550 pounds of convenience meals that may be contaminated with Listeria monocytogenes, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.

The following products are subject to recall:

"10.3-ounce packages of "7-ELEVEN FRIED CHICKEN BENTO"
"11-ounce packages of "7-ELEVEN TERIYAKI CHICKEN BENTO"
"10-ounce packages of "7-ELEVEN BREAKFAST SCRAMBLE BOWL"
"17.75-ounce packages of "7-ELEVEN BIG BENTO"
"7.25-ounce packages of "7-ELEVEN LITTLE SMOKIES SNACK PACK"

Each package includes a best eaten by date and time of "06/30/11 11:30 AM". The packages also bear "EST. 12444" or "P-12444" inside the USDA mark of inspection. The products were produced on June 28, 2011 and distributed to retail stores in Hawaii.

The problem was discovered as a result of microbiological testing conducted by FSIS and may have occurred as a result of the products becoming cross-contaminated through contact with a food scale pan. FSIS and the company have received no reports of illnesses associated with consumption of these products.



Follow us on "twitter" for instant updates on recalls, recipes, and food tips. @thechefjohnny

Dietary Supplements




From the U.S. Food and Drug Administration



Dietary Supplements: What You Need to Know!



Q What are dietary supplements?
A
Dietary supplements include vitamins, minerals, and other less familiar substances — such as herbals, botanicals, amino acids, enzymes, and animal extracts (see box at right). Dietary supplements are also marketed in forms such as tablets, capsules, softgels, and gelcaps. While some dietary supplements are well understood and established, others need further study.

Q What are the benefits of dietary supplements?
A
Some supplements can help assure that you get an adequate dietary intake of essential nutrients; others may help you reduce the risk of disease. However, supplements should not replace the variety of foods that are important to a healthful diet — so, be sure you eat a variety of foods as well.

Unlike drugs, supplements are not intended to treat, diagnose, prevent, or cure diseases. That means supplements should not make claims, such as "reduces arthritic pain" or "treats heart disease." Claims like these can only legitimately be made for drugs, not dietary supplements.

Q Are there any risks in taking supplements?
A
Yes. Many supplements contain active ingredients that have strong biological effects in the body. This could make them unsafe in some situations, and hurt or complicate your health. For example, the following actions could lead to harmful — even life-threatening — consequences.

Combining supplements:
Using supplements with medications (whether prescription or over-the-counter)
Substituting supplements for prescription medicines
Taking too much of some supplements, such as vitamin A, vitamin D, and iron
Some supplements can also have unwanted effects before, during, and after surgery. So, be sure to inform your health-care provider, including your pharmacist, about any supplements you are taking — especially before surgery.

Q Who's responsible for the safety of dietary supplements?
A
Dietary supplements are not approved by the government for safety and effectiveness before they are marketed. If the dietary supplement contains a NEW ingredient, that ingredient will be reviewed by FDA (not approved) prior to marketing — but only for safety, not effectiveness.

The manufacturers and distributors of dietary supplements are responsible for making sure their products are safe BEFORE they go to market. Manufacturers are required to produce dietary supplements in a quality manner and ensure that they do not contain contaminants or impurities, and are accurately labeled.

Manufacturers will also be required to report all serious dietary supplement related harmful effects or illnesses to FDA starting January, 2008. FDA can take dietary supplements off the market if they are found to be unsafe or if the claims on the products are false and misleading.

Q How can I find out more about the dietary supplement I'm taking?
What should I do if I have a reaction to a dietary supplement?
A You, your health-care provider, or anyone else should report a serious problem from the use of any dietary supplement directly to FDA's MedWatch Program at:

1-800-FDA-1088
(toll-free phone number)
1-800-FDA-0178
(fax)
The FDA Safety Information and Adverse Event Reporting Program3

FDA would like to know whenever the use of a dietary supplement causes you to have a serious reaction or illness, even if you're not certain that the product was the cause, and/or you did not visit a doctor or clinic.
A If you want to know more about the product you are taking, check with the manufacturer or distributor about:

Information to support the claims of the product
Information on the safety and effectiveness of the ingredients in the product

Any reports of adverse effects or events from consumers using the product

Q How can I be a smart supplement shopper?
A
Although the benefits of some dietary supplements have been documented, the claims of others may be unproven. If something sounds too good to be true, it usually is.

Be a savvy supplement user. Here's how:

Watch out for false statements like:
A quick and effective "cure-all"
Can treat or cure diseases
"Totally safe" or has "no side effects"
Be aware that the term natural doesn't always mean safe.
Don't assume that even if a product may not help you, at least it won't hurt you.
When searching for supplements on the Web, use the sites of respected organizations, rather than doing blind searches.
Ask your health-care provider for help in distinguishing between reliable and questionable information.
Always remember — safety first!

Tuesday, July 5, 2011

South Carolina Firm Recalls Ham Products for Possible Listeria Contamination

Recall Release CLASS I RECALL
FSIS-RC-046-2011 HEALTH RISK: HIGH


WASHINGTON, July 5, 2011- Carolina Pride Foods, Inc., a Greenwood, S.C. establishment is recalling approximately 18,416 pounds of boneless, fully cooked ham products that may be contaminated with Listeria monocytogenes, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.

All the ham products were produced on May 13, 2011 and then distributed throughout the southeastern U.S. to retail outlets or for institutional use.

The following products are subject to recall:

"10-ounce vacuum packages of "CAROLINA PRIDE Smoked Diced Ham" with the sell by date of Sept. 23, 2011 stamped on the package. The packages also bear "EST. 242" inside the USDA mark of inspection and were sent to retail locations in Alabama, Florida, Georgia, North Carolina, South Carolina and Tennessee. The label on 10-pound cases of this product would be stamped "4218."
"10-pound cases containing five, 2-pound vacuum packages of "CAROLINA PRIDE Diced Ham." The label on cases of this product would be stamped "3804" and shipped to locations in North Carolina, South Carolina and Georgia.
"12-pound cases containing 8-ounce vacuum packages of "HARDEE's Smoked Diced Ham" with the use through date of Nov. 9, 2011 stamped on the package. The shipping label on cases of this product would be stamped "4181" and shipped to locations in Florida, Georgia, North Carolina and South Carolina.

Maritime Services Available

For the past eight years, we have been training the ServSafe® course to stewards and cooks, as well as other aspects of safe, efficient, and cost effective galley operations. Our firm also assists in the updating and development of Steward Department Operations Policy Manuals and Steward Crew member handbooks using the current FDA Food Code. Training food safety to the maritime steward department takes more than being proficient in the training process. Knowing the maritime industry, understanding the steward department’s everyday operation and applying sound food safety principles to address the on-board challenges is critical to proper training. If your maritime company needs on-board or on-shore food safety training, contact us at 321-567-4644.

Monday, June 27, 2011

Cantaloupes Recalled

FOR IMMEDIATE RELEASE - June 24, 2011 - Scottsdale, AZ - Eagle Produce, LLC of Scottsdale, Arizona has announced a limited recall of certain cantaloupes shipped from Arizona to upstate New York in late Mayhttp://www.fda.gov/Safety/Recalls/ucm260820.htm