WebJul 20, 2024 · Ethicon Endo-Surgery Inc. 4545 Creek Rd. Blue Ash OH 45242-2803. For Additional Information Contact. SAME. 513-337-7000. Manufacturer Reason. for Recall. An internal component may be cracked and become lodged behind the energy button potentially resulting in continuous activation of the device, may result in burns. WebMay 2, 2024 · Ethicon’s Auris Health subsidiary received the FDA clearance for Monarch for endourological procedures. Company officials say it’s now the first and only multispecialty, flexible robotic...
FDA takes action to protect women’s health, orders manufacturers …
WebU.S. Food & Drug Administration 10903 New Hampshire Avenue Doc ID# 04017.06.00 Silver Spring, MD 20993 www.fda.gov March 15, 2024 Ethicon Endo-Surgery ... leveraged from Ethicon Endocutters, and new 3-D B-shaped final staple form into the new ECHELON LINEARTM Cutter Reload as shown in illustration 5-1. Ethicon Endo-Surgery, LLC WebThis report does not reflect a conclusion by ethicon, or its employees that the report constitutes an admission that the product, ethicon, or its employees caused or contributed to the potential event described in this report. ... U.S. Food and Drug Administration. 10903 New Hampshire Avenue Silver Spring, MD 20993 Ph. 1-888-INFO-FDA (1-888-463 ... buford roof replacement
MAUDE Adverse Event Report: ETHICON INC. SURGICEL …
WebAll Ethicon Products Adjunctive Hemostats Digital Solutions Energy Sealing & Dissecting LINX Reflux Management MONARCH™ Platform Neuwave Microwave Ablation Surgical Stapling Vascular Access & Infection Control Wound Closure Other Products Order Support CA Compliance Contributions and Donations Clinical & Technical Support Education Grants WebU.S. Food & Drug Administration 10903 New Hampshire Avenue Doc ID# 04017.04.32 Silver Spring, MD 20993 www.fda.gov April 8, 2024 Ethicon Endo-Surgery, LLC ... Company: Ethicon Endo-Surgery, LLC. 475 Calle C Guaynabo, PR 00969 . Contact: Ekta Patel Senior Regulatory Affairs Specialist Ethicon Endo-Surgery, Inc. Phone: WebETHICON INC. VCL+ VIO 27IN 2-0 S/A UR-6 SUTURE, ABSORBABLE, SYNTHETIC: Back to Search Results: Model Number VCP602H: ... Date FDA Received: 03/30/2024: Is this an Adverse Event Report? No Is this a Product Problem Report? Yes Device Operator: Device Model Number: VCP602H: Device Catalogue Number ... buford roy cannon sr. texas