Department of JusticeU.S. Attorney’s OfficeEastern District of Oklahoma FOR IMMEDIATE RELEASEFriday, April 5, 2024 MUSKOGEE, OKLAHOMA – The United States Attorney’s Office for the Eastern District of Oklahoma announced that Rebecca Elaine Holloway, age 33, of Oklahoma City, Oklahoma, was sentenced to 12 months in prison for one count of Tampering with Consumer Products, a violation…
Global Mix, Inc Recalls Tejocote Products Because of Possible Health Risk
Summary Company Announcement Date: April 05, 2024 FDA Publish Date: April 10, 2024 Product Type: Dietary SupplementsFood & Beverages Reason for Announcement: Recall Reason Description Product contains toxic yellow oleander. Company Name: Global Mix, Inc. Brand Name: Brand Name(s) Eva Nutrition, Science of Alpha, Niwali, NWL Nutra Product Description: Product Description Tejocote Dietary Supplements Company…
Home Style Foods, Inc. Issues Allergy Alert on Undeclared Egg in Kowalski Simply Sides – Jack’s Potato Salad
Summary Company Announcement Date: April 10, 2024 FDA Publish Date: April 10, 2024 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared Egg Company Name: Home Style Foods, Inc. Brand Name: Brand Name(s) Kowalski Simply Sides Product Description: Product Description Jack’s Potato Salad Company Announcement Home Style Foods, Inc., of Hamtramck,…
Oregon Spice Company Issues Allergy Alert on Undeclared Sesame in Johnny’s Parmesan Garlic Seasoning
Summary Company Announcement Date: April 10, 2024 FDA Publish Date: April 10, 2024 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared Sesame Company Name: Oregon Spice Company Brand Name: Brand Name(s) Johnny’s Product Description: Product Description Parmesan Garlic Seasoning Company Announcement April 10, 2024, Oregon Spice Company, Portland, OR is…
Baron Spices, Inc. Issues Allergy Alert on Undeclared Soy and Wheat in Blues Hog Sweet & Savory Seasoning
Summary Company Announcement Date: April 09, 2024 FDA Publish Date: April 09, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential or Undeclared Allergen – Soy and Wheat Company Name: Baron Spices, Inc. Brand Name: Brand Name(s) Product Description: Product Description Company Announcement Baron Spices, Inc. of St. Louis, MO is…
Belgian Yummies Issues Allergy Alert on Undeclared Allergens of Wheat, Soy, Egg, Coconut and/or Peanuts and FD&C Yellow #5 in Ice Cream Sandwiches and Gelato
Summary Company Announcement Date: April 09, 2024 FDA Publish Date: April 09, 2024 Product Type: Food & Beverages Ice Cream/Frozen Dairy Allergens Reason for Announcement: Recall Reason Description Undeclared Wheat, Soy, Egg, Coconut &/or Peanuts, FD&C Yellow #5 Company Name: Belgian Yummies Brand Name: Brand Name(s) Belgian Yummies, SOFRA, Ria Product Description: Product Description Ice…
Medline Industries, LP Issues a Nationwide Recall of Convenience Kits Containing Nurse Assist 0.9% Sodium Chloride Irrigation USP and Sterile Water for Irrigation USP
Summary Company Announcement Date: April 05, 2024 FDA Publish Date: April 08, 2024 Product Type: Medical Devices Reason for Announcement: Recall Reason Description The potential for a lack of sterility Company Name: Medline Industries, LP Brand Name: Brand Name(s) Medline and Centurion Product Description: Product Description Convenience kits Company Announcement Northfield, Ill., Apr. 5, 2024…
Medos International Sàrl Recalls Cerenovus CEREBASE DA Guide Sheath due to Cracking of the Distal Catheter Shaft
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Names: CERENOVUS CEREBASE DA Guide Sheath, Part Numbers: GS9070SD; GS9080SD; GS9090SD; GS9095SD; Neurovascular guide catheter, single-use Product Codes: QJP Manufacturing Dates: July 7,…
Honeywell Safety Products USA, Inc. Issues Voluntary Worldwide Recall of Honeywell Fendall 2000 Non-Sterile Eyewash Cartridges # 32-002050-0000 used with the Fendall 2000 Eyewash Station Due to a Lack of Appropriate Policies and Procedures by Honeywell’s Supplier
Summary Company Announcement Date: April 04, 2024 FDA Publish Date: April 05, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Non-compliance with current good manufacturing practice (cGMP) requirements. Company Name: Honeywell Safety Products USA Brand Name: Brand Name(s) Fendall 2000 Product Description: Product Description Non-Sterile Eyewash Cartridge Company Announcement FOR IMMEDIATE RELEASE –…
Aruba Aloe Balm N.V. Issues Voluntary Nationwide Recall of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel Due to Presence of Methanol
Summary Company Announcement Date: April 05, 2024 FDA Publish Date: April 05, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Product contains methanol Company Name: Aruba Aloe Balm N.V. Brand Name: Brand Name(s) Aruba Aloe Product Description: Product Description Hand Sanitizer Gel and Alcoholada Gel Company Announcement FOR IMMEDIATE RELEASE – April 5th,…