Class 2 Device Recall Stryker | 合法醫療器材資訊網

2020年1月15日 — Recall Status, Terminated on August 31, 2020 ... Product, Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or ... Read More

2020年6月16日 — Stryker issued Urgent Medical Device Recall (UMDR) - PFA 2365134 letter on May 7, 2020 to affected US consignees by third-party recall ... Read More

2020年4月24日 — On April 13, 2020, a Product Recall Notification letter was sent to all affected customers (Distributors and Branches/Agencies). The firm instructed ... Read More

Stryker has had to recall some of its products because of concern for patient safety. The company has paid billions of dollars to end metal-on-metal hip implant ... Read More

Last Modified: July 29, 2020. Fact Checked ... Stryker had recalled nearly 44,000 Rejuvenate and 9,000 ABG II implants in April 2012. The company sent out an ... Read More

Stryker Hip Replacement Recalls ... Stryker hip implant recalls occurred after reports revealed fretting, corrosion and other complications in patients implanted with ... Read More

This contact form is for recall questions only. For other inquiries, please ... To request recall information from Stryker, complete the form below. First name *. Read More

2020年11月9日 — Stryker Neurovascular is recalling the Trevo XP ProVue Retriever device because there is a risk the core wire may break or separate when the ... Read More

Officials at the Stryker Corporation initiated a worldwide recall of the Rejuvenate, ABG II and LFIT Anatomic V40 Femoral Head due to serious problems including​ ... Read More