FDA Class II · Medical device · May 27, 2026
Tangent Endoscopy recall — TANGENT ENDOSCOPY, LLC
Affected devices exhibited fractures at the distal shaft tip without complete detachment.
Official ID Z-2209-2026 · Official record ↗
Recall found. TANGENT ENDOSCOPY is named in FDA Class II recall Z-2209-2026 covering Tangent Endoscopy. Hazard: Affected devices exhibited fractures at the distal shaft tip without complete detachment. Identifying details: (1) Model Number: TNG4002-IND; UDI-DI: (1) 00850061601001; Lot numbers: 2510900, 2512938, and 2601944. (2) Model Number: TNG-4007-6pk; UDI-DI: 00850061601001; Lot numbers: 2510900, 2512938, and 2601944. Status: Ongoing.
Affected devices exhibited fractures at the distal shaft tip without complete detachment.
Official ID Z-2209-2026 · Official record ↗
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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.