Drug recall
Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.
FDA recall event 98654 · Class II · TANGENT ENDOSCOPY, LLC
Key facts
| Event ID | 98654 |
|---|---|
| Recall numbers | Z-2209-2026 |
| Recalling firm | TANGENT ENDOSCOPY, LLC |
| Product type | Devices |
| Products | Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Affected devices exhibited fractures at the distal shaft tip without complete detachment. |
| Initiation date | Mar 23, 2026 |
| Report date | May 27, 2026 |
| City | Camden |
| State | DE |
| Country | United States |
| FEI number | 3041659934 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: