Domega NY International Co., Ltd Issues an Alert on Undeclared Sulfites in Green Day Brand White Melon Seeds

Domega NY International Co., Ltd. at 47-57 Bridgewater Street Brooklyn New York 11222 is recalling GREEN DAY BRAND WHITE MELON SEEDS because they contain undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
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Olaax Corp. Issues a Nationwide Voluntary Recall of All Lots of Maxiloss Weight Advanced Softgels Dietary Supplement

Olaax Corp announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplement sold under the brand name MAXILOSS WEIGHT ADVANCED softgels to the user level because they contain undeclared Sibutramine. Olaax Corp. is conducting a voluntary recall after being notified by the US FDA that testing found the MAXILOSS WEIGHT ADVANCED product, to contain Sibutramine.

FDA alerts health care providers of recall of anemia drug Omontys

The U.S. Food and Drug Administration is alerting health care providers and patients of a voluntary nationwide recall of all lots of Omontys Injection by Affymax, Inc., of Palo Alto, Calif., and Takeda Pharmaceuticals Company Limited, of Deerfield, Ill., due to reports of anaphylaxis, a serious and life-threatening allergic reaction. Omontys is used to treat anemia in adult dialysis patients.

Affymax and Takeda Announce a Nationwide Voluntary Recall of All Lots of OMONTYS® (peginesatide) Injection

Affymax, Inc. (Nasdaq: AFFY) and Takeda Pharmaceutical Company Limited (Takeda) today have decided to voluntarily recall all lots of OMONTYS® (peginesatide) Injection to the user level as a result of new postmarketing reports regarding serious hypersensitivity reactions, including anaphylaxis, which can be life-threatening or fatal. The companies have been working actively with the U.S. Food and Drug Administration (FDA) which has indicated its agreement with this decision.