Modular Neck Stem Voluntary Recall Information | 合法醫療器材資訊網

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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

This contact form is for recall questions only. For other inquiries, please review this page for additional points of contact. recall ... Read More

2020年11月9日 — Reason for Recall ... Stryker Neurovascular is recalling the Trevo XP ProVue Retriever device because there is a risk the core wire may break or ... 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

Results 401 - 500 of 500 — Stryker Howmedica Osteonics Corp. Trident Acetabular System Surgical Protocol. Instructions for use of hip prosthesis. Literature Num... Read More

2020年1月15日 — Action, Stryker issued Urgent Medical Device Recall - PFA 2147264 letter dated November 7, 2019) to US consignees by third-party recall ... Read More

This voluntary recall was initiated due to potential risks associated with modular-neck stems. These risks include the potential for fretting and/or corrosion ... Read More

2020年11月11日 — Stryker recalls device for treating blood clots after 1 death, 11 injuries ... Stryker has recalled a device intended to treat blood clots during ... Read More