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Model Number 31202 |
Device Problem
Patient-Device Incompatibility (2682)
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Patient Problems
Adhesion(s) (1695); Unspecified Infection (1930); Pain (1994); Scar Tissue (2060); Hernia (2240); Obstruction/Occlusion (2422)
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Event Type
Injury
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Manufacturer Narrative
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We are unable to fully investigate this event as no product code, lot number, or sample was provided.This report is based upon allegations made in a lawsuit in which atrium medical is named as a defendant.
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Event Description
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This event is deemed reportable based on the allegations in a lawsuit which, while unsubstantiated, suggest that a reportable event may have occurred during use of atrium medical¿s mesh product.Plaintiff allegedly experienced severe injury, adhesions, hematoma, infection, recurrent hernia, pain, additional medical care and treatment or surgery.Since this is a legal matter, the case has been turned over to legal counsel and further information obtained through investigation or discovery may fall under the attorney/client and/or work product privilege.However, atrium will supplement this report as appropriate if additional information comes to its attention.
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Manufacturer Narrative
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Based on the review of the device history and sterilization records and product complaint details atrium can find no fault with the product.This lot of mesh passed all quality and performance requirements.
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Event Description
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Plaintiff also allegedly abdominal pelvic lavage, enterotomy, experienced scar tissue, loops of bowel obstructions, incarceration, drainage, abdominal wall reconstruction, seroma, murky brown liquid and vac placement.
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Search Alerts/Recalls
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