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Tubes, Gastrointestinal (And Accessories)

FDA product code KNT · Class 2 · Gastroenterology, Urology

8,266
Registered devices
25,839
Adverse events
268
Recalls
651
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-04-30Avanos Medical, Inc.Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30Avanos Medical, Inc.Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30Avanos Medical, Inc.Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30Avanos Medical, Inc.Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30Avanos Medical, Inc.Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30Avanos Medical, Inc.Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30Avanos Medical, Inc.Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30Avanos Medical, Inc.Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30Avanos Medical, Inc.Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30Avanos Medical, Inc.Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.