The Food and Drug Administration issued the Interstate Certified Shellfish Shippers List (ICSSL) for August. The ICSSL is published monthly for the information and use by food control officers, the seafood industry and other interested persons. The shippers listed have been certified by regulatory authorities in the U.S., Canada, Chile, South Korea, Mexico and New Zealand under the uniform sanitation requirements of the National Shellfish Program.
On Aug. 12 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Aug. 11 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
During the week of Aug. 4-10, the Food and Drug Administration modified the following existing Import Alerts (not otherwise listed on the FDA's new and revised import alerts page) on the detention without physical examination and/or surveillance of:
On Aug. 8 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
The Food and Drug Administration will allow use of vitamin D3 as a food additive in certain meal replacement beverages, it said in a final rule that takes effect Aug. 12. The agency says it will allow Vitamin D3 as a nutrient supplement, subject to limitations on the total amount, in meal replacement beverages that are not intended for special dietary use in reducing or maintaining body weight and for use in foods that are sole sources of nutrition for enteral feedings. Objections and requests for hearings are due Sept. 11.
On Aug. 7 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
The Food and Drug Administration issued its weekly Enforcement Report for Aug. 6 that lists the status of recalls and field corrections for food, drugs, biologics, and devices. The report covers both domestic and foreign firms.
A New York seafood importer faces import alert and possible seizures after the Food and Drug Administration found it to be in violation of seafood hazard analysis and critical control point (HACCP) regulations, according to an agency warning letter dated July 22. FDA says it refused admission of an entry imported by H.A.R. Maspeth Corp. after routine sampling detected salmonella. A subsequent inspection found that the company isn’t taking action to ensure the dried squid it imports is processed in accordance with seafood HACCP rules, said FDA. The agency warned H.A.R. Maspeth that if the violations aren’t corrected, the company’s seafood imports may be detained without physical examination or seized. FDA also said it may assess fees to cover the costs of any reinspection to verify compliance.
On Aug. 6 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of: