This article needs additional citations for verification. (January 2015)
Ethicon, Inc. is a subsidiary of Johnson & Johnson. It was incorporated as a separate company under the Johnson & Johnson umbrella in 1949 to expand and diversify the Johnson & Johnson product line.
|Formerly||G.F.Mersons Limited, Ethicon Suture Laboratories|
|Industry||Surgical systems and instruments|
|Founder||George F. Merson|
|Headquarters||Bridgewater, New Jersey and Cincinnati, Ohio|
|Michael Del Prado (chairman)|
Andrew Ekdahl (President)
|Products||Prolene, Monocryl, Vicryl, Ethilon, Gynecare|
|Revenue||$4.87 billion (sales) (2011)|
Number of employees
|Parent||Johnson & Johnson|
Ethicon has manufactured surgical sutures and wound closure devices since 1887. After World War II, Ethicon's market share in surgical sutures rose from 15% to 70% worldwide. In the United States, the market share is approximately 80%.
Ethicon conducts business in 52 countries.
In 1915, George F. Merson opened a facility in Edinburgh for the manufacturing, packaging and sterilising of catgut, silk and nylon sutures. Johnson & Johnson acquired Mr. Merson's company in 1947, and this was renamed Ethicon Suture Laboratories. In 1953 this became Ethicon Inc.
In 2013, J&J merged Ethicon Endo-Surgery back into Ethicon.
Physiomesh Class Action LawsuitsEdit
On June 13, 2016, Health Canada issued a recall of Ethicon's Physiomesh Flexible Composite Mesh Product used for ventral hernia repair. The product had been on the Canadian market since September 2010 and patients claimed a range of complications following surgery. The proposed Canadian class action, filed June 1, 2017 is seeking court approval for certification as a class action and is expected to proceed in 2019.
Gynecare Prolift controversyEdit
There is some controversy around Ethicon's transvaginal meshes used on patients with female genital prolapse.
Ethicon's Gynecare Prolift, was introduced in March 2005, bypassing FDA review. The company felt its basic polypropylene had already been approved and therefore it did not need to reapply for clearance for its Prolift kit. Three years later, when Ethicon tried to obtain clearance for its Prolift +M, the FDA was alerted to the fact that Prolift had been on the market. The agency approved the Prolift and Prolift +M with no penalty. Both were cleared through the Food and Drug Administrations 510(k) clearance process, that is clearance to sell. Ethicon's parent company Johnson & Johnson utilized the FDA's 510(k) clearance method, which allows a product to be sold without official FDA approval if it is based on another already approved product. However, in 2008, the FDA issued a Public Health Notification regarding reports of serious complications associated with transvaginal mesh devices. This escalated in 2011 when the agency received more than 1,000 adverse effect reports from surgical mesh manufacturers. The FDA decided to order Ethicon and other transvaginal mesh manufacturers to cease production until extensive testing and research on each of vaginal mesh device was conducted. In June 2012, following the FDA's order for additional testing, Johnson & Johnson permanently removed all Prolift products from the market.
In one court case reported by Reuters, the plaintiff, Dianne Bellew, on whom the product had been implanted in 2009, said she was never warned about how the device could contract and erode, causing pain and scarring.
- "Locations around the world". Ethicon U.S. Retrieved 25 January 2016.
- Perriello, Brad (22 May 2014). "J&J's pipeline includes 30 'major' medical devices and a surgical robot". MassDevice. Retrieved 25 January 2016.
- "Management's Discussion and Analysis of Results of Operations and Financial Condition" (PDF). Johnson & Johnson. 2011. p. 29. Archived from the original (PDF) on 2 February 2016. Retrieved 25 January 2016.
- "ETHICON History". Ethicon Products.co.uk. Archived from the original on 10 January 2016. Retrieved 25 January 2016.
- "A history of advancing surgery". Ethicon U.S. Retrieved 25 January 2016.
- Arnold, Matthew (8 May 2013). "J&J consolidates, rebrands Ethicon units". Medical Marketing & Media.
- Garde, Damian (30 July 2013). "KCI buying ex-J&J unit for $485M". FierceBiotech. Retrieved 2020-11-10.
- "Johnson & Johnson Completes $1.07 bln. Acquisition Of Mentor". RTTNews. 23 January 2009. Retrieved 2020-11-10.
- Krauskopf, Susan Kelly, Lewis (2008-12-01). "J&J to buy breast implant firm Mentor for $1.1 billion". Reuters. Retrieved 2020-11-10.
- "J&J Inhales Sinus Device Maker for $785M". Forbes. Retrieved 2020-11-10.
- Brunsman, Barrett (14 April 2016). "Ethicon acquires maker of cancer-killing devices". Cincinnati Business Courier.
- "Health Canada Physiomesh Recall". Health Canada. Retrieved 7 February 2019.
- "Canadian Patients Join Class Action Lawsuit Over Hernia Mesh". CTV News. Retrieved 7 February 2019.
- "Physiomesh (Hernia Mesh) Class Action Lawsuit". Murphy Battista LLP. Retrieved 7 February 2019.
- Linda Gross Prolift Trial Atlantic City, NJ Superior Court, 2013.
- "Ethicon Gynecare Prolift Mesh - Vaginal Mesh Lawsuit". Girard Gibbs. Retrieved 1 October 2017.
- "Week Ahead in Health: March 2, 2015". Reuters. 2 March 2015. Retrieved 1 October 2017.