CONTACT: JEFF WARREN INVESTOR RELATIONS 763-505-2696 CHUCK GROTHAUS PUBLIC RELATIONS 763-505-2614 MEDTRONIC, INC. (NYSE: MDT) ANNOUNCED THAT THE U.S. FOOD AND DRUG ADMINISTRATION (FDA) CLASSIFIED AS CLASS I ITS VOLUNTARY RECALL ACTION INITIATED ON FEBRUARY 11, 2009 OF ITS BIOGLIDE VENTRICULAR SNAP SHUNT CATHETER (CAT. #S 27782, 27708 AND 27802) … [Read more...]
Search Results for: catheter
Atrium Initiates Voluntary Recall Action Regarding HYDRAGLIDE Brand Heparin-Coated Thoracic Drainage Catheters
CONTACT: ATRIUM 1-800-5-ATRIUM FOR IMMEDIATE RELEASE -- HUDSON, NEW HAMPSHIRE – MAY 12, 2008 – ATRIUM MEDICAL CORPORATION TODAY ANNOUNCED THAT IT IS INITIATING A VOLUNTARY AND PRECAUTIONARY RECALL OF SELECTED LOTS OF HYDRAGLIDE™ BRAND HEPARIN-COATED THORACIC DRAINAGE CATHETERS. LIMITED LOTS OF ATRIUM HEPARIN-COATED HYDRAGLIDE … [Read more...]
Urgent Recall Alert – Endologix Visiflex Catheters
Endologix, Inc. today announced the limited voluntary recall of 30 Visiflex™ bifurcated delivery catheters for its Powerlink® System (models 25-16-155BL and 28-16-155BL) located at seven customer sites. Based on a single field occurrence due to the failure of a catheter component manufactured by a third party, the Company has determined that these … [Read more...]
BD Announces Voluntary Worldwide Recall for One Lot of ChloraPrep™ Clear 1 mL Applicators Due to Fungal Contamination
Summary Company Announcement Date: January 31, 2025 FDA Publish Date: February 18, 2025 Product Type: Drugs … [Read more...]
Baxter Issues Voluntary Nationwide Recall of One Lot of Heparin Sodium 0.9% Sodium Chloride Injection Due to Potential for Elevated Endotoxin Levels
Summary Company Announcement Date: August 05, 2024 FDA Publish Date: August 06, 2024 Product Type: Drugs … [Read more...]
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