In case of failure, this may cause a potential delay in using the SJT in the Axilla area
San Diego, CA (PRWEB) October 13, 2014
AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Junctional Tourniquet.
The US FDA announced on October 8, that SAM Junctional Tourniquet Accessory (Axilla) Strap, by SAM Medical Products, is recalled due to potential clip failure. SAM Junctional Tourniquet is approved for controlling pelvic fracture stabilization, axilla hemorrhage, and inguinal hemorrhage.
The reason for the recall is a potential issue with a clip used to secure the accessory strap used for the Axilla application of the SAM Junctional Tourniquet (SJT). In case of failure, this may cause a potential delay in using the SJT in the Axilla area. Inguinal hemorrhage and pelvic fracture indications of the SJT are not impacted by this issue.
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 Junctional Tourniquet 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 “SAM Medical Products has notified customers of the voluntary recall by letter and is arranging with its customers to rapidly replace the current axilla straps with an updated version.”
AttorneyOne.com has further information on Junctional Tourniquet at the website including the latest major drug, food, and medical products law news.
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