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Diamondback 360 Peripheral Orbital Atherectomy System Recalled (Class I): AttorneyOne Monitors and Keeps Consumers Informed - Valley News Live - KVLY/KXJB - Fargo/Grand Forks

Diamondback 360 Peripheral Orbital Atherectomy System Recalled (Class I): AttorneyOne Monitors and Keeps Consumers Informed

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On August 19, the FDA announced that certain lots of the Diamondback 360 Peripheral Orbital Atherectomy Systems, by Cardiovascular Systems, are recalled because they may contain sheath that can fracture during use. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers.

San Diego, CA (PRWEB) August 22, 2014

AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Diamondback 360 Peripheral Orbital Atherectomy System.

The US FDA announced on August 19, that certain lots of the Diamondback 360 Peripheral Orbital Atherectomy Systems, model number DPB-125MICRO145 (Part number 7-10003), by Cardiovascular Systems, are recalled because they may contain defective saline sheaths that could fracture during use and could possibly block blood vessels. Diamondback 360 Peripheral Orbital Atherectomy System is a high-speed cutting tool inserted via a catheter into blood vessel and it is used to reestablish blood flow in narrowed arteries or arterio-venous dialysis shunts.

The affected lots are: 100573, 100575, 100674, 100676, 100678, 100680.

The FDA classified this recall as Class I, meaning use of the products included in the recall may cause serious injuries or death.

Taking into consideration the latest developments, AttorneyOne.com monitor daily and update the website providing accurate information on all relevant FDA safety alerts. Sean Burke, director of Media Relations at AttorneyOne.com, adds we are determined to keep an eye on FDA announcements concerning Diamondback 360 Peripheral Orbital Atherectomy System and inform the public. For that reason", he continues, "our focus should squarely fall on investigating these safety alerts and getting the word out.

As the FDA notes On May 27, 2014, Cardiovascular Systems sent an 'Urgent Medical Device Recall' letter to their customers. The letter identified the problem and the specific products affected by the recall. The letter advises customers to:

  • Remove affected devices from service.
  • Complete and return a 'Customer Acknowledgement Form.'
  • Return affected devices to Cardiovascular Systems

AttorneyOne.com has further information on Diamondback 360 Peripheral Orbital Atherectomy System at the website including the latest major drug, food, and medical products law news.

Headquartered in San Diego, CA Attorney One was founded in 2004 and is not a law firm. They offer a nationwide legal service which helps consumers find the best representation for their legal needs. You can learn more about Attorney One at our website http://www.attorneyone.com. You can also find us on Facebook at http://www.facebook.com/AttorneyOne. Checkout earlier news from us at http://www.prweb.com/releases/2014/08/prweb12110809.htm

For the original version on PRWeb visit: http://www.prweb.com/releases/2014/08/prweb12114014.htm

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