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列表文章資訊參考來源
Class 3 Device Recall Restorelle DirectFix Posterior Mesh
2012年5月2日 — Coloplast is conducting a field correction based on the conclusion that two lots of Restorelle DirectFix Posterior mesh were mislabeled. The ... ...（以下省略）
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2012年5月2日 — Coloplast is conducting a field correction based on the conclusion that two lots of Restorelle DirectFix P...
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2024年4月11日 — The complications associated with the use of surgical mesh slings marketed at the time for SUI repair wer...
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Vaginally placed mesh has a significant risk of severe complications, including mesh erosion, pain, infection, and bladd...
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2019年4月17日 — Deborah Kotz at the FDA informs Mesh News Desk that the Y-shape mesh is still marketed for the treatment ...
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2018年10月5日 — The Restorelle mesh lawsuit was filed by a couple from California, alleging the companies failed to warn ...
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2019年7月11日 — Restorelle Polypropylene Mesh (2019-07-11). Starting date: July 11 ... Type II; Source of recall: Health ...
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Indications: Restorelle Y is indicated for use as a bridging material for sacrocolposuspension/sacrocolpopexy (transabdo...
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Adverse events following mesh implantation may be de novo, persistent, worsening, transient, or permanent. Potential com...
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TGA Recall Reference ... Coloplast urogynaecological surgical mesh. Aris Kit ARTG Number: 157074. Altis System ARTG Numb...
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2019年5月17日 — A recall was issued by Boston Scientific Corporation Pty Ltd on 2 May 2019, RC-2019-RN-00681-1 to remove ...
restorelle y mesh recall 參考影音
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