Medical DeviceMar 20, 2019
US Endoscopy Group US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock recall — FDA Z-1011-2019
Potential esophageal laceration during a patient procedure
Class IIFDA: TerminatedUS Endoscopy Group Inc.
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies US Endoscopy Group Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.