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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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Stryker Hip Implant Recall | 合法醫療器材資訊網
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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
Recall | 合法醫療器材資訊網
This contact form is for recall questions only. For other inquiries, please review this page for additional points of contact. recall ... Read More
Stryker Neurovascular Recalls Trevo XP ProVue Retriever ... | 合法醫療器材資訊網
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
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
Medical Device Recalls | 合法醫療器材資訊網
Results 401 - 500 of 500 — Stryker Howmedica Osteonics Corp. Trident Acetabular System Surgical Protocol. Instructions for use of hip prosthesis. Literature Num... Read More
Class 2 Device Recall Stryker Orthopaedics | 合法醫療器材資訊網
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
Modular Neck Stem Voluntary Recall Information | 合法醫療器材資訊網
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
Stryker recalls device for treating blood clots after 1 death | 合法醫療器材資訊網
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
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