Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

Smith & Nephew Grasper, Cupped 3.4mm REF: 011014

FDA Recall Z-0973-05 · Posted 2005-07-07

Recalling FirmSmith & Nephew, Inc., Endoscopy Div.
Recall StatusTerminated
Product CodeGDJ
Date Initiated2005-04-06
Date Terminated2006-06-07
Product Quantity12

Reason for Recall

Cupped Grasper Handle marked incorrectly as Duckbill Upbiter

Firm Action

Smith & Nephew Endoscopy notified users by letter dated 4/6/05. Accounts are requested to return product.

Root Cause

Other

Distribution Pattern

CA, OH, MA, TX

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑