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What Stryker hips have been impacted by the FDA recall | 合法醫療器材資訊網

What Stryker hips have been impacted by the FDA recall

OfficialsattheStrykerCorporationinitiatedaworldwiderecalloftheRejuvenate,ABGIIandLFITAnatomicV40FemoralHeadduetoseriousproblemsincluding​ ...

 What Stryker hips have been impacted by the FDA recall

The numerous recalls of hip implants over the years in the US were due to a high rate of failure and injury to patients.

“Metal-on-metal” wear and tear is a common cause of failure, as the metal components of the implant rub against each other, releasing metallic debris into the surrounding tissue and causing inflammation, pain, and potential damage to muscles, bones, and nerves.

Do you suspect you need revision surgery due to a defective hip implant? The personal injury attorneys at Rosenfeld Injury Lawyers, LLC, are advocates for injured patients harmed by defective medical devices.

Contact defective medical device lawyers[1] at (888) 424-5757 to schedule a free consultation and discuss your legal options for initiating a hip implant case. We have experience with Stryker hip replacement lawsuits.

ABG II and Rejuvenate Devices

The FDA approved...

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Class 2 Device Recall Stryker Orthopaedics | 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
Class 2 Device Recall Stryker | 合法醫療器材資訊網
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
Class 2 Device Recall Stryker Spine | 合法醫療器材資訊網
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 Corporation – History | 合法醫療器材資訊網
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
Stryker Hip Lawsuit | 合法醫療器材資訊網
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 Implant Recall | 合法醫療器材資訊網
Stryker Hip Replacement Recalls ... Stryker hip implant recalls occurred after reports revealed fretting, corrosion and other complications in patients implanted with ... Read More
Recall | 合法醫療器材資訊網
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
Stryker Neurovascular Recalls Trevo XP ProVue Retriever ... | 合法醫療器材資訊網
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
What Stryker hips have been impacted by the FDA recall | 合法醫療器材資訊網
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
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