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

OfficialsattheStrykerCorporationinitiatedaworldwiderecalloftheRejuvenate,ABGIIandLFITAnatomicV40FemoralHeadduetoseriousproblemsincluding ...

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...

Recalled Stryker Hip Implants | 合法醫療器材資訊網

Stryker Corporation – History | 合法醫療器材資訊網

The first LFIT V40 lawsuit is scheduled for trial in 2019. Pending Lawsuits Against Stryker. Rejuvenate and AGB II Hip Implants. Number of Lawsuits: 1,240 lawsuits ... Read More

Stryker Hip Lawsuit | 合法醫療器材資訊網

As of August 2019, there were nearly 2,000 Stryker hip replacement lawsuits in ... Stryker had recalled nearly 44,000 Rejuvenate and 9,000 ABG II implants in ... 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

Class 2 Device Recall C2 Nerve monitor | 合法醫療器材資訊網

2019年10月1日 — for Recall, Stryker C2 NerveMonitor's design and instructions may not ... On July 31, 2019, the firm distributed an Urgent Medical Device Recall ... Read More

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

Date Initiated by Firm, September 12, 2019. Create Date, March 17, 2020. Recall Status, Open, Classified. Recall Number, Z-1509-2020. Recall Event ID, 85100 ... 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

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

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

Stryker Hip Recall – Lieff Cabraser | 合法醫療器材資訊網

2021年6月24日 — Stryker Hip Injuries & Device Recall. Issue: Recalled Rejuvenate and ABG II hip implants ... What Is The Stryker Hip Recall Settlement? Read More

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