Source: FDA | Recall date: 05/27/2026
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Affected product: Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.
Summary: Affected devices exhibited fractures at the distal shaft tip without complete detachment.
Hazard: Affected devices exhibited fractures at the distal shaft tip without complete detachment.
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