![]() ![]() We are committed to providing you with the most recent and accurate product information and will update this site on an as needed basis. 1 System components include ECHELON FLEX Powered Plus Stapler and ENDOPATH ECHELON Reloads with Gripping Surface Technology. ![]() Knowledgeable buyers are expected to carefully review all of the available information in the inspection report, including all photographs, in order to make the best bidding and buying decision possible. Before using any medical device, review all relevant package inserts with particular attention to the indications, contraindications, warnings and precautions, and steps for use of the device (s). The Ethicon Circular Stapler (ILS) with its controlled tissue compression and Adjustable Height Staple Technology is designed to deliver optimal compression. This inspection report includes ratings, comments, and photos of the various components of the item. In 2019, Ethicon issued recalls of several types of surgical stapler for misfiring. These inspections are not designed nor intended to detect latent defects, or conditions that could only be found in connection with the physical dismantling of the equipment or the use of diagnostic tools or techniques. This in turn can cause serious injuries or even death in the patients on whom a misfiring stapler was used. We are their clinical and technical lifeline for Ethicon products.' Michelle Kellogg, MSN, BA, RN, CSM, CQM- Lead Analyst, Ethicon Resource Nurse. Please note that IronPlanet inspections are performed solely for the purpose of reporting the visible condition of the equipment's major systems and attachments on the day of the inspection and do not include load testing or digging/lifting. 'Customers can reach out to us in the middle of a procedure 24/7 and talk to a Nurse or Biomed who can assist them with their questions. Following submission of a written dispute claim, IronPlanet will investigate the claim, re-inspecting the equipment item as necessary, and determine a fair and mutually beneficial resolution. With IronClad Assurance®, if a buyer discovers that the item is not substantially in the condition as represented in this inspection report, the buyer may submit a written dispute claim to IronPlanet. The surgical staplers were manufactured between Maand March 6, 2019, and distributed between Maand March 8, 2019.Disputes: This item is offered with IronClad Assurance® protection. The following product codes are involved in this Class 1 Recall: CDH21A, CDH25A, CDH29A, CDH33A, ECS21A, ECS25A, ECS29A and ECS33A. ![]() ETHICON ENDOPATH 33 and ETHICON PROXIMATE 33 Stapler (ECS33, CDH33, SDH33) 1BSGC3334. ![]() ETHICON ENDOPATH 29 and ETHICON PROXIMATE 29 Stapler (ECS29, CDH29, SDH29) 1BSGC2829. The Johnson & Johnson Medical Devices Companies comprise the surgery, orthopedics, and interventional solutions businesses within Johnson & Johnsons Medical Devices segment. ETHICON ENDOPATH 25 and ETHICON PROXIMATE 25 Stapler (ECS25, CDH25, SDH25) 1BSGC25. All other trademarks are the property of their respective owners. This recall involves a total of 92,496 Endo-Surgery Curved and Endo-Surgery Endoscopic Curved Intraluminal Staplers with adjustable height staples that are designed to permit a proper matching of the staples to the diameter of the lumen in gastrointestinal surgeries. is the legal manufacturer of ECHELON FLEX Powered Staplers. The FDA describes that Class I Recalls are reserved for “situations in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death”. The Ethicon Endo-Surgery Curved Intraluminal Stapler (and its endoscopic variation) and Echelon Flex Endopath Stapler are surgical staplers that are commonly. (a subsidiary of Johnson & Johnson), for various defects which can increase the risk of severe injury or even death to patients undergoing treatment with the products. On May 15, 2019, the FDA issued a Class 1 Recall for a pair of surgical stapler devices manufactured by Ethicon, Inc. ![]()
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