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…
Baloian Farms of Arizona Co., Recalls Whole Fresh American Cucumbers Because of Possible Health Risks Due to Salmonella
Summary Company Announcement Date: November 29, 2024 FDA Publish Date: December 02, 2024 Product Type: Food & Beverages Produce Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Salmonella Company Name: Baloian Farms of Arizonia Co., Inc. Brand Name: Brand Name(s) Product Description: Product Description Whole Fresh American Cucumbers Company Announcement Nogales,…
Baker Farms Recalls Baker Brand Curly Mustard Due to Listeria Monocytogenes Contamination
Summary Company Announcement Date: December 02, 2024 FDA Publish Date: December 02, 2024 Product Type: Food & Beverages Produce Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Listeria monocytogens Company Name: Baker Farms Brand Name: Brand Name(s) Baker Farms Product Description: Product Description Curly Mustard Greens Company Announcement Norman Park, GA…
Russ Davis Wholesale Recalls Multiple Products Due to Potential Salmonella Risk
Summary Company Announcement Date: December 01, 2024 FDA Publish Date: December 02, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness/Salmonella Company Name: Russ Davis Wholesale Brand Name: Brand Name(s) Crazy Fresh and more Product Description: Product Description Cucumbers and salads with kit Company Announcement Russ Davis…
Insertion Tube Recall: FHC Removes microTargeting Insertion Tube Sets due to a Manufacturing Size Error That May Lead to Patient Harm
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: microTargeting Insertion Tube Set Unique Device Identifier (UDI)/Product Model: 10873263004323/66-IT-05P Lot Number: 244517…