Food & Drug Packaging Press Releases - EIN Presswire - Press Release Distribution Service

Published on January 5, 2026 - 21:34 GMT

Esophageal pH Monitoring Capsule Recall: Medtronic and Given Imaging Remove Bravo CF Capsule Delivery Devices

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 The FDA is aware that …

Distribution channels: Food & Beverage Industry

Published on January 5, 2026 - 21:34 GMT

Diagnostic Intravascular Catheter Recall: Conavi Removes Novasight Hybrid Catheters

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 The FDA is aware that …

Distribution channels: Food & Beverage Industry

Published on January 5, 2026 - 21:34 GMT

Infusion Pump Software Recall: Baxter Removes Sigma Spectrum Infusion System Platforms

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 Spectrum V6 infusion …

Distribution channels: Food & Beverage Industry

Published on January 5, 2026 - 21:34 GMT

Intravascular PICC Catheter Recall: Bard Removes PowerPICC Intravascular Catheters

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 The FDA is aware that …

Distribution channels: Food & Beverage Industry

Published on January 2, 2026 - 23:53 GMT

Custom Surgical Pack Recall: Alcon Removes Custom Pak Ophthalmic Procedure Packs

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 The FDA is aware that …

Distribution channels: Food & Beverage Industry

Published on December 30, 2025 - 16:21 GMT

Intravascular Administration Set Recall: ICU Medical Removes IV Gravity Burette Set

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 Affected Item Numbers …

Distribution channels: Food & Beverage Industry

Published on December 30, 2025 - 14:50 GMT

Anesthesia System Correction: GE HealthCare Updates Use Instructions for CareStation Anesthesia Systems

This recall involves updating instructions for using 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 …

Distribution channels: Food & Beverage Industry

Published on December 29, 2025 - 20:06 GMT

Continuous Glucose Monitoring Software Correction: Dexcom Issues Correction for Dexcom G6 and G6 Pro Software

This recall involves correcting devices and does not involve removing the 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 without …

Distribution channels: Food & Beverage Industry

Published on December 27, 2025 - 06:28 GMT

Gold Star Distribution Inc., Issues Recall of Certain FDA-Regulated Products in Three States Including Drugs, Devices, Cosmetics, ...

Summary Company Announcement Date: December 26, 2025 FDA Publish Date: December 26, 2025 Product Type: Animal & Veterinary Cosmetics Dietary Supplements Drugs Food & Beverages Medical Devices Foodborne Illness Reason for Announcement: Recall Reason …

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Published on December 25, 2025 - 01:15 GMT

Consumers Supply Distributing, LLC Recalls Country Vet Biscuits for Dogs Due to Possible Salmonella Health Risk

COMPANY ANNOUNCEMENT When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Read Announcement View Product Photos …

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Published on December 24, 2025 - 00:54 GMT

Gregory’s Foods Issues Allergy Alert on Undeclared Peanuts in "Bag Full of Cookies" White Chocolate Macadamia Nut Frozen Cookie ...

COMPANY ANNOUNCEMENT When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Read Announcement View Product Photos …

Distribution channels: Food & Beverage Industry

Published on December 23, 2025 - 21:48 GMT

Atwater’s Issues Allergy Alert on Undeclared Tree Nut Allergen on Cookie Tin Labels

COMPANY ANNOUNCEMENT When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Read Announcement View Product Photos …

Distribution channels: Food & Beverage Industry

Published on December 23, 2025 - 21:47 GMT

Recall Notice: Willy Pete’s Chocolate Company LLC of Harwinton Issues Recall of Chocolate Bars Due to Almonds Not Declared in ...

COMPANY ANNOUNCEMENT When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Read Announcement View Product Photos …

Distribution channels: Food & Beverage Industry

Published on December 23, 2025 - 21:47 GMT

Silvestri Sweets Expands Voluntary Allergy Alert on Undeclared Pecan and Wheat in Cookie Butter Holiday Bark and Pecan, Cranberry &...

COMPANY ANNOUNCEMENT When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Read Announcement View Product Photos …

Distribution channels: Food & Beverage Industry

Published on December 23, 2025 - 21:46 GMT

Catheter Mount Recall: Draeger Removes ErgoStar Catheter Mounts

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 The FDA is aware that …

Distribution channels: Food & Beverage Industry

Published on December 23, 2025 - 21:46 GMT

Endovascular Graft Recall: Cook Medical Removes Zenith Alpha 2 Thoracic Endovascular Graft

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 The FDA is aware that …

Distribution channels: Food & Beverage Industry

Published on December 23, 2025 - 18:36 GMT

Early Alert: Convenience Kit Needle Issue from Integra LifeSciences

The FDA has become aware of a potentially high-risk device issue. The FDA will keep the public informed and update this web page as significant new information becomes available. Affected Product The FDA is aware that Integra LifeSciences has issued a …

Distribution channels: Food & Beverage Industry

Published on December 23, 2025 - 18:36 GMT

MRI System Correction: Siemens Healthineers Issues Correction for 3 Tesla MRI Systems

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 …

Distribution channels: Food & Beverage Industry

Published on December 23, 2025 - 18:36 GMT

System Correction: IMPRIS Imaging Inc Issues Correction for IMRIS Neuro III-SV

This recall involves correcting 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 …

Distribution channels: Food & Beverage Industry

Published on December 23, 2025 - 00:28 GMT

Troemner Roemner Farm Issues Allergy Alert on Undeclared Milk, Wheat, and Soy in Pfeffernusse Cookies

COMPANY ANNOUNCEMENT When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Read Announcement View Product Photos …

Distribution channels: Food & Beverage Industry