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VIA

US Endoscopy · Model 00717262 · UDI-DI 00816765016237

NWU Prescription
3
510(k) clearances
19
Adverse events
23
Recalls
37
Facilities

Description

The VIA procedure kit custom includes transport pad, gauze, biohazard sticker, water detergent label, solidifier, Chux pad, basin, dry sponge, enzymatic sponge, lubricant jelly, syringe, DuoSwift brush, BioGuard 4-piece kit, BioGuard air water cleaning adapter, and O2 CO2 tubing.

Recalls

DateFirmReason
2026-03-19Medline Industries, LPDuring an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o
2025-09-04American Contract Systems Inc.Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not
2025-07-14American Contract Systems IncDuring an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further
2025-02-11MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may
2025-02-06American Contract Systems IncACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
2025-02-06American Contract Systems IncACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
2025-01-31American Contract Systems, Inc.Sterility assurance with procedure trays
2024-11-21MEDLINE INDUSTRIES, LP - NorthfieldCustom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
2024-11-08Cardinal Health 200, LLCPotential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
2024-11-08Cardinal Health 200, LLCPotential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.