Class IIOngoingZ-2209-2026
TANGENT ENDOSCOPY, LLC recalls Tangent Endoscopy
Affected devices exhibited fractures at the distal shaft tip without complete detachment.
TANGENT ENDOSCOPY, LLCDEMay 27, 2026
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–2 of 2 recalls
Affected devices exhibited fractures at the distal shaft tip without complete detachment.
Potential for inadvertent retention of biomaterial when the reprocessing procedure is not performed as instructed, so as not completely removing and disassembling the device.