[3-13-2024] FDA reminds consumers not to purchase or use Govvi WOW!. FDA laboratory analysis confirmed an additional sample of Govvi WOW! contained undeclared DMHA, in addition to 1,4 DMAA. DMHA is also known as “1,5-dimethylhexylamine,” “1,5-DMHA,” “2-amino-6-methylheptane,” “2-aminoisoheptane,” and “octodrine.” Use of DMHA can elevate blood pressure and could contribute to cardiovascular problems, including heart…
John B. Sanfilippo & Son, Inc Issues Allergy Alert on Undeclared Coconut and Milk in Great Value Honey Roasted Cashews 8.25 Oz
Summary Company Announcement Date: March 12, 2024 FDA Publish Date: March 13, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared milk and coconut allergens Company Name: John B Sanfilippo & Son, Inc. Brand Name: Brand Name(s) Great Value Product Description: Product Description Honey Roasted Cashews Company Announcement FOR IMMEDIATE RELEASE…
Abbott Recalls HeartMate Touch Communication System for Unintentional Pump Start and Stop
Please be aware, this recall is a correction, not a product removal. 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: HeartMate Touch Communication System Product Codes: See Recall Database Entry Distribution…
Par Pharmaceutical Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection Due to Potential for Silicone Particulates in the Product Solution
Summary Company Announcement Date: March 12, 2024 FDA Publish Date: March 12, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Potential Presence of Silicone Particulate Matter Company Name: Endo International, Par Pharmaceutical Brand Name: Brand Name(s) Par Pharmaceutical Product Description: Product Description Treprostinil 20mg/20mL Injection Company Announcement FOR IMMEDIATE RELEASE – March 12,…
Windstone Medical Packaging, Inc. Recalls Local Lower Extremity Pack, In House Ocular Pack and Closure Kit Containing Sterile Water Based Products Under Recall by Nurse Assist
Please be aware, this recall is a correction, not a product removal. 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: Local Lower Extremity Pack, In House Ocular Pack and Closure Kit Product Codes:…
La Fiesta Food Products Recalls Cinnamon Ground Because of Possible Health Risk
Summary Company Announcement Date: March 06, 2024 FDA Publish Date: March 08, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Metal Contaminant – Lead Company Name: La Fiesta Food Products Brand Name: Brand Name(s) Product Description: Product Description Ground Cinnamon Company Announcement 03/06/2024, La Fiesta Food Products, La Mirada California…
Wesco, Inc. Issues Voluntary Recall and Allergy Alert on Undeclared Peanut in Wesco Mint No Bake Cookie Bites
Summary Company Announcement Date: March 08, 2024 FDA Publish Date: March 11, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Peanut Allergen Company Name: Wesco, Inc. Brand Name: Brand Name(s) Wesco Fresh Product Description: Product Description Mint No Bake Cookies Company Announcement Wesco, Inc. of Muskegon, MI is recalling 750…
Ventec Life Systems Recalls VOCSN Patient Breathing Package (Pediatric, Active, Oxygen, Blue) for Manufacturing Issue with Bonded Spiral Wrap
Please be aware, this recall is a correction, not a product removal. 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: VOCSN Patient Breathing Package (Pediatric, Active, Oxygen, Blue) Product Code: CBK Model Numbers:…
Cardinal Health Recalls Sterile Monoject Luer-Lock and Enteral Syringes Due to a Change in Manufacturing
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: Cardinal Health Monoject sterile Syringe Luer-Lock Tip Soft Packs (1, 3, 6, 12, 20, 35, and 60 mL) Cardinal Health Monoject sterile Enteral Syringes with…
Raja Foods Skokie, IL Is Recalling “Swad Brand Cinnamon Powder 3.5OZ Retail Packs” for Possible Lead Contamination
Summary Company Announcement Date: March 06, 2024 FDA Publish Date: March 07, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Metal Contaminant – Lead Company Name: Raja Foods LLC Brand Name: Brand Name(s) Product Description: Product Description Cinnamon Powder Company Announcement Raja Foods LLC of Skokie, Il is recalling its…