FDA recall notice for The Rheo Knee bionic prosthetic is to be used exclusively for fittings of lower extremity amputations. RHEO KNEE uses Artificial Intellig
FDA recall notice for Ossur Lil Angel Vest P3 Sorbatex. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders
FDA recall notice for Ossur Lil Angel Vest P3 Kodel. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders r
FDA recall notice for Ossur Lil Angel Vest P2 Kodel. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders r
FDA recall notice for NecLoc Extrication Collar Product Usage: Necloc collars are applied to patients afflicted with cervical injuries to ensure immobilizat
FDA recall notice for Miami J Collar Product Usage: Miami J collars are applied to patients afflicted with cervical injuries to ensure immobilization. (Ossu
FDA recall notice for Extreme Custom Product Usage: Extreme Custom is an external knee braces to provide support for knee instability due to ligament injuri
FDA recall notice for Unloader XT Product Usage: Unloader XT Extreme is an external knee braces to provide support for knee instability due to ligament inju
FDA recall notice for Back Support Suspenders Clip on Black Back Support Suspenders Sew on Black (Ossur H / F). Reason: Ossur Americas is recalling , Knee Shie
FDA recall notice for Knee Undersleeve Gray Product Usage: Knee undersleeves are worn as an accessory for comfort under knee braces. (Ossur H / F). Reason:
FDA recall notice for Rebound Cartilage Product Usage: Rebound Cartilage is an external knee brace that provides support for knee instability due to ligamen
FDA recall notice for Rebound Cartilage Custom Product Usage: Rebound Cartilage Custom is an external knee brace that provides support for knee instability
FDA recall notice for Unloader Custom Lite Product Usage: Unloader Custom Lite is an external knee braces to provide support for knee instability due to li
FDA recall notice for Rebound Air Walker Product Usage: Rebound Air Walkers are indicated for grade 2 and grade 3 ankle sprains, to stabilize fractures, pos
EU Safety Gate recall notice for BPATA (PAKETA). Reason: The rocket is not stable and may shoot in the wrong direction causing injuries…. Issued 2018-01-19.
EU Safety Gate recall notice for Secret gift (Unknown). Reason: The time measured between the ignition of the firework and the explosion of the…. Issued 2018-01
EU Safety Gate recall notice for Top Gun (Slysavarnarfélagið Landsbjörg). Reason: The instructions for use of the stabilization flaps situated under the product
EU Safety Gate recall notice for Sling Unlimited 4 in 1 (Mini Monkey). Reason: The attachment system can easily slip and the product can break. Issued 2019-05-0