Class II

Medical Device Recall: Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.

TANGENT ENDOSCOPY, LLC · March 23, 2026

Reason for Recall

Affected devices exhibited fractures at the distal shaft tip without complete detachment.

Distribution

US Nationwide distribution in the states of North Carolina, Arizona, and Nevada.

States Affected

NATIONWIDE

Quantity Affected

53 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2209-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

TANGENT ENDOSCOPY, LLC Medical Device Recall: Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk. | SafeCheck