Summary Company Announcement Date: December 06, 2024 FDA Publish Date: December 06, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description May be contaminated with Salmonella Company Name: Fresh Creative Foods Brand Name: Brand Name(s) Fresh Creative Foods Product Description: Product Description The Beef & Lamb Gyro Sandwich Express Meal Kits Company…
Neonatal Incubator Correction: GE HealthCare Updates Use Instructions for GE HealthCare Giraffe OmniBed Carestation and Incubator Carestation due to Risk of Patient Formaldehyde Exposure
The devices described in this recall are the same devices announced in the related Letter to Health Care Providers. On November 8, 2024 the FDA issued an update to the Letter to Health Care Providers to provide the most recent recommendations provided by GE HealthCare. This recall involves updating instructions for using devices, and does…
Atkinson Milling Company Recalls Frozen 1 Lb Bag Frozen Hushpuppies with Onions, 2 Lb 8oz Bag Frozen Hushpuppies With Onions and 2 Lb 8oz Bag Frozen Hushpuppies Without Onions Due to Undeclared Milk
Summary Company Announcement Date: December 05, 2024 FDA Publish Date: December 05, 2024 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Potential or Undeclared Allergen – Milk Company Name: Atkinson Milling Company Brand Name: Brand Name(s) Atkinson’s Product Description: Product Description Hushpuppies with Onions, Hushpuppies Company Announcement SELMA, NC – December…
Former EMT Sentenced for Drug Tampering
Department of JusticeU.S. Attorney’s OfficeWestern District of Tennessee FOR IMMEDIATE RELEASEThursday, December 5, 2024 Memphis, TN – A Cordova, Tennessee woman has been sentenced to a year and a day in federal prison for tampering with a vial of Benadryl while on duty as an Emergency Medical Technician. Reagan Fondren, Acting United States Attorney for the Western…
Supreme Service Solutions LLC Voluntarily Recalls Supreme Produce Cucumber Products Because of Possible Health Risk
Summary Company Announcement Date: December 04, 2024 FDA Publish Date: December 05, 2024 Product Type: Food & Beverages Produce Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness/Salmonella Company Name: Supreme Produce Brand Name: Brand Name(s) Supreme Produce Product Description: Product Description Mutiple items with cucumbers Company Announcement Reason for Announcement: Potential to…
Walmart Inc. Recalls Marketside Fresh Cut Cucumber Slices in 34 Texas Stores Because of Possible Health Risk
Summary Company Announcement Date: December 03, 2024 FDA Publish Date: December 04, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness/Salmonella Company Name: Walmart Inc. Brand Name: Brand Name(s) Marketside Product Description: Product Description Cut cucumber slices Company Announcement BENTONVILLE, Ark. Dec. 3, 2024 – Following a…
Yummi Sushi LLC Voluntarily Recalls Cucumber Products Because of Possible Health Risk
Summary Company Announcement Date: December 04, 2024 FDA Publish Date: December 05, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness/Salmonella Company Name: Yummi Sushi LLC Brand Name: Brand Name(s) Yummi Sushi Product Description: Product Description Multiple sushi products with cucumber Company Announcement Reason for Announcement: Potential…
JFE Franchising, Inc. Recalls A Limited Number of Cucumber Products Because Of Possible Health Risk
Summary Company Announcement Date: December 04, 2024 FDA Publish Date: December 04, 2024 Product Type: Food & Beverages Produce Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness/Salmonella Company Name: JFE Franchising, Inc. Brand Name: Brand Name(s) Snowfruit Snowfox Product Description: Product Description Multiple products with cucumbers Company Announcement Houston, TX (December 4,…
Syringe Recall: Cardinal Health Removes Certain Monoject U-100 mL Insulin Syringe Luer Lock with Tip Cap Soft Packs due to Incompatibility with Needleless Connectors
This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected Product Product Names: Monoject U-100 mL Insulin Syringe Luer Lock with Tip Cap Soft Pack (extended…
Peritoneal Dialysis Set Correction: Baxter Issues Correction for MiniCap Extended Life Peritoneal Dialysis Transfer Sets Due to Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBA and/or NDL-PCBs
This recall involves correcting certain devices, and does not involve removing them from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it without correction. Affected Product Product Name: MiniCap Extended Life PD Transfer…